What's On Your Plate

Undeclared Soy Protein in Aunt Jemima Frozen Pancakes

noreply@blogger.com (WOYP) — Sun, 29 Jan 2012 21:42:00 +0000

If you have Soy Protein sensitivity, this alert is importance to you. Pinnacle Foods Group LLC is recalling certain Aunt Jemima Frozen Pancakes, as they may contain this undeclared allergen. This recall was initiated after the Company discovered potential cross-contact of this product with one containing soy protein being produced on the same equipment.

This recall applies only to: “AUNT JEMIMA FROZEN PANCAKES” packaged in cardboard cartons with the UPC codes listed below. These cartons were sold and distributed nationally and have a ‘Recommended Use By Date’ between November 1, 2011 and October 16, 2012.

Production Code information is as follows:

Retail UPC Code	Description
19600-05100	AUNT JEMIMA PANCAKES BUTTERMILK LOW FAT 12/14.5oz
19600-05490	AUNT JEMIMA OATMEAL PANCAKES 12/14.8oz
19600-05820	AUNT JEMIMA PANCAKES BUTTERMILK 12/14.8oz
19600-05910	AUNT JEMIMA PANCAKES HOMESTYLE 12/14.8oz
19600-05955	AUNT JEMIMA CONFETTI PANCAKES 12/14.8oz
19600-06040	AUNT JEMIMA WHOLE GRAIN PANCAKES 12/14.5oz

If you are not allergic to soy protein, this product is safe to eat. If you are allergic to or have a severe sensitivity to soy protein, you should not consume this product. Please return the product to the store where purchased for a full refund.

Consumers with questions may contact the Company at 1- 888-299-7646 daily between 9 a.m. and 8 p.m. ET. The Food and Drug Administration has been made aware of this recall.

Photo Courtesy: FDA

Anytime Deli Brand Turkey & Ham Footlong Sandwich Recalled: Listeria Contamination

noreply@blogger.com (WOYP) — Tue, 24 Jan 2012 17:23:00 +0000

Anytime Deli Turkey & Ham Sub Sandwich, UPC 0543200194, with an expiration date of January 19th and January 22nd has been recalled because it might be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

The sub sandwiches were distributed on January 2nd and 3rd to convenience stores in Florida and South Georgia. The sandwich is packaged in white butcher wrap. Though no illnesses have been reported, the recall was the result of a routine sampling program by the Florida Department of Agriculture and Consumer Services.

The product has already been removed from store shelves. However, consumers who may have purchased the sandwich for later consumption are urged to return it to the place of purchase for a full refund.

Consumers with questions may contact the company at 1-800-394-6258 Monday through Friday 8:00 AM to 5 PM EST.

Photo Courtesy: FDA

Jones’ Seasoning Voluntarily Recalls Original and Spicy Southwest Blend Mock Salt

noreply@blogger.com (WOYP) — Mon, 23 Jan 2012 18:26:00 +0000

Jones’ Seasoning Blends LLC announced a voluntary recall of Jones’ Mock Salt Original and Jones’ Mock Salt Spicy Southwest Blend due to the potential contamination of Salmonella. This recall has been initiated by the Company due to possible Salmonella contamination of the celery seeds ingredient used in Jones Mock Salt. The supplier of the celery seeds has placed a recall for the seeds and Jones Seasoning Blends LLC has also taken every action possible in notifying the public.

Markets in California, Minnesota, and Washington were sold the products directly. They were also sold through internet orders on www.jonesmocksalt.com:

Jones’ Mock Salt Original: Organic Salt Free Seasoning, 1.6 oz bottles (UPC 0 94922 16616 6), 12 oz bags (UPC 0 94922 07199 6) and 16 oz bags (0 94922 16616 6).
Jones’ Mock Salt Spicy Southwest Blend: Organic Salt Free Seasoning, 1.6 oz bottles (UPC 0 94922 01560 0).

There is no lot number identifying the bottles or bags. Any products purchased from July 1, 2011 to December 14, 2011 should be destroyed.

Consumers should contact Ms. June Jones on how to receive replacements:
Ph: 253-468-9595 (Monday-Friday 8:00 am - 5:00 pm PST)
Email: jonesseasoningblends@gmail.com

Russia Bans Fresh Vegetable Imports from EU

noreply@blogger.com (WOYP) — Thu, 02 Jun 2011 18:40:00 +0000

In the light of the European E.Coli crisis, Russia has announced that it was banning imports of raw vegetables from the European Union because of the E. coli outbreak. The head of the Russian consumer protection agency Gennady Onishchenko said that that ban came into effect this morning. This is a development from the ban placed on vegetable imports by Russia on Germany and Spain last month.

You may also wish to read:
Story: Two in U.S. infected in European E. coli Outbreak
Story: WHO - European E.Coli Update

WHO: European EColi Update

noreply@blogger.com (WOYP) — Thu, 02 Jun 2011 13:36:00 +0000

The WHO has reported that the E. coli strain responsible for the deadly outbreak in Europe is a new bacteria that has never been seen before. Preliminary genetic sequencing by scientists suggests that the strain is a mutant form of two different E. coli bacterium. The genes contained within it are highly virulent and produce a lethal toxin. This maybe the reason why this outbreak is so extensive and dangerous.

Hilde Kruse, a food safety expert at the World Health Organization, said:

this is a unique strain that has never been isolated from patients before

Today on its website, the WHO noted 10 countries in Europe including Sweden, Austria, Denmark, France, Netherlands, Norway, Spain, Switzerland and the United Kingdom have all reported patients with two disease related to the bacteria: haemolytic uraemic syndrome (HUS) and enterohemorrhagic E. coli (EHEC). It is believed that 17 people in Germany, and sickened more than 1,500 others, including 470 who have developed a rare kidney failure complication. It further said that as of May 31, nine patients in Germany had died of HUS and six of EHEC, and one person in Sweden had also died. There are many hospitalized patients, several of them requiring intensive care, including dialysis.

Investigations are continuing into the cause of the outbreak, which is at present unclear.

Source: Various

You may also wish to read:
Story: Two in U.S. infected in European E. coli outbreak
Story: Russia Bans Fresh Vegetable Imports from EU

Two US Residents Infested in European E.Coli Outbreak

noreply@blogger.com (WOYP) — Wed, 01 Jun 2011 18:43:00 +0000

Two U.S. residents who traveled in northern Germany may have been affected by the massive outbreak of food poisoning in Europe. Federal health officials confirmed Tuesday that the victims have been hospitalized with serious, life-threatening complications of E. coli infections.

The deputy director of food borne, bacterial and mycotic diseases at the U.S. Centers for Disease Control and Infection observed that:

we have never seen that organism before

The American victims have not yet been identified by name or state.

The FDA say is also flagging incoming produce especially cucumbers, lettuce and tomatoes from Spanish growers implicated in the outbreak for further inspection.

Del Bueno Recalls Cheese Because Of Possible Health Risk

noreply@blogger.com (WOYP) — Thu, 18 Nov 2010 17:25:00 +0000

Del Bueno of Grandview, WA has recalled all size packages of the foollowing cheeses manufactured by them:

Queso Fresco Fresh Cheese
Queso Panela Fresh Cheese
Requeson Mexican Style Ricotta Cheese
Queso Enchilado Dry Cheese

This recall is the result of environmental samples and finished product samples taken by Food and Drug Administration (FDA) as well as the finished product samples taken by Washington State Department of Agriculture (WSDA). The test results revealed that the cheeses are contaminated with Listeria monocytogenes.

Listeria monocytogenes contamination can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Symptoms include largely short-term symptoms such as fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. However, Listeria infection can cause miscarriages and stillbirths among pregnant women.

UPC dates of the products being recalled are as follows:

Queso Fresco Fresh Cheese, UPC 75318225028 for 16 oz. package, UPC 753182814063 for 3 lbs. package, date code up to and including Feb 10 2011.
Queso Panela Fresh Cheese, UPC 753182814056, date code up to and including Feb 10 2011.
Requeson Mexican Style Ricotta Cheese, UPC 753182814070, date code up to and including Jan 10 2011
Queso Enchilado Dry Cheese, no UPC date code up to and including Mar 15 2011.

These c heeses were distributed by Del Bueno to retail markets in Washington and Oregon and to the flea market in Pasco, WA. You can find the expiration date code stamped on the back of the packages. The cheese is packaged either in 1 lb. or 3 lbs. plastic vacuum bags. Del Bueno has notified their customers and has pulled the products from retail stores and the company is working with FDA to conduct the recall. If you have purchased Del Bueno brand cheeses are urged to return them to the place of purchase for a full refund.
Contact:
Del Bueno
Jesus Rodriguez
425-503-3823 (8am-5pm PST)

Image Source: FDA

Liz Lovely Voluntary Recall Chocolate Products: Undeclared Dairy

noreply@blogger.com (WOYP) — Sun, 14 Nov 2010 17:26:00 +0000

Liz Lovely, Inc. of Waitsfield, VT, a dairy free bakery, has recalled recalling cookie products containing chocolate or chocolate chips. Chocolate purchased from a third-party chocolate manufacturer has undeclared dairy present in it.

Liz Lovely cookie products are distributed nationwide in retail stores and through mail orders. People wirh dairy allergy are at risk of serious or life-threatening allergic reaction if they consume these undeclared dairy affected products.

This voluntary recall includes Products with the following UPC:

Cowboy Cookies 6oz. Plastic Bag With 2 Cookies 893410000018 00497, 00504, 0051
Cowgirl Cookies 893410000056 00493, 00503, 0051
Peanut Butter Classics 893410000025 00496, 0050
Gluten Free Chocolate Fudge 893410001008 00499, 00415, 0051
Gluten Free Triple Choc. Mint 893410001122 0050
Gluten Free Chocolate Chip 893410001015 0050
Lovely Oh's 8oz. Plastic Clamshell Container 893410002111 00501, 0051
Mint Lovely Oh's 893410002159 00501, 0051
Peanut Butter Lovely Oh's 893410002289 00501, 0051
Organic Pretzels 893410002081 00501, 00513

It is important to note that, the lot number for the 6oz. plastic bags is stamped on each 12-unit case box, not printed on each package. Lot number for the 8oz. containers is printed on a sticker affixed to each unit, along with a best-by date.

The recall was initiated after one allergic reaction to dairy was reported. Production will resume on November 24, 2010 with 100% dairy free chocolate and updated product packaging. If you any of these products in a retail store or had them shipped between October 4, 2010 and November 15, 2010, you are urged to return them to the place of purchase for a full refund.

More Information @: Voluntary Recall

Contact:
Dan Holtz
802-793-4956 (8am-5pm EST)
www.lizlovely.com

Source: FDA

E.coli Contamination in Gorgonzola Cheese Sold at Costco

noreply@blogger.com (WOYP) — Thu, 11 Nov 2010 17:40:00 +0000

Colorado State health department officials have issued a warning to consumers who purchased Mauri Gorgonzola Cheese @ Costco with sell by dates January 13, 2011, and January 14, 2011. E. Coli O157:H was found in an unopened package that was tested at the state health department's lab. Consequently, its distributor, DPI Specialty Foods of Tualatin, Ore., has issued a recall for this product.

Consumers should note that this cheese was sold only at the Costco stores in Colorado. It is packaged in clear plastic in 1 lb. wedges and can be identified by information contained on a white sticker on the package: DISTRIBUTED BY DPI Specialty Foods Tualatin, OR, ITALY 34449" with sell by dates of "01/13/11" or "01/14/11." The Costco item number is 34449.

The FDA advises consumers against eating this cheese. You can return it to the place of purchase or dispose of it in a closed plastic bag. Place the bag in a sealed trash can that prevents people and animals (including wild animals), from eating the product.

The FDA advises that E. coli O157:H7 infection can lead to diarrhea and abdominal cramps. While most people recover within a week, some may develop a severe infection. Rarely, a type of kidney failure called hemolytic uremic syndrome can occur (as symptoms of diarrhea improve); this can happen at any age but is most common in children under 5 years old and in older adults. People with hemolytic uremic syndrome should be hospitalized immediately, as their kidneys may stop working and they may be at risk for other serious health problems.

State health officials urge persons with signs or symptoms of E. coli O157:H7 to contact their health care provider. The latter should immediately report any suspected infection to state or local public health authorities.

Costco has removed the cheese from its stores and using card purchase records, has notified consumers by phone of the situation.

Contact:
Lori Maldonado
Deputy Director, Office of Communications
Colorado Department of Public Health and Environment
Cell: 303-921-8598
Email: lori.maldonado@state.co.us

Consumers with questions contact DPI Specialty Foods @: 1-800-597-3876.

Source: FDA

Elie Baking Corp. Alert: Soy in Food City Low-Carb Tortilla

noreply@blogger.com (WOYP) — Tue, 17 Aug 2010 05:20:00 +0000

The Elie Baking Corp. of Brockton, Mass has issued an allergy alert on its Food City brand Low-Carb Tortilla White and Whole Wheat 10 count. This is due to the presence of undeclared soy in the products.

Details of Recall:

Food City brand, Low Carb Tortilla White, 13.5 oz, 10 count. UPC 0 87848 42002 0
Food City brand, Low Carb Tortilla Whole Wheat, 13.5 oz.10 count. UPC 0 87848 42003 0
MFG Date 07/21/10 & MFG Date 07/22/10 stamped on the top left of the bag.

Consumers are asked to note that people who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products The products were distributed in K-VA-T Food Stores, Inc. d/b/a Food City retail stores, in the following states: Kentucky, Virginia, and Tennessee. SP far, no illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that product containing soy was distributed in packaging that did not declare soy in the ingredient statement. Consumers who have purchased Food City low Carb Tortilla White & Whole Wheat 10 ct are urged to return them to the place of purchase for a full refund.

Contact: dianag@neareastbakery.com
Call collect: 508 584 4890
Monday through Friday from 9:00 am to 5:00 pm

Image Source: FDA

Iowa Company Issues Egg Recall in USA

noreply@blogger.com (WOYP) — Sun, 15 Aug 2010 05:39:00 +0000

Wright County Egg has issued the following statement regarding the US Food and Drug Administration’s (FDA) on-farm records review and egg testing for Salmonella.

"Wright County Egg of Galt, Iowa is voluntarily recalling specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis or arthritis.

Eggs affected by this recall were distributed to food wholesalers, distribution centers and foodservice companies in California, Illinois, Missouri, Colorado, Nebraska, Minnesota, Wisconsin and Iowa. These companies distribute nationwide.

Eggs are packaged under the following brand names: Lucerne, Albertson, Mountain Dairy, Ralph’s, Boomsma’s, Sunshine, Hillandale, Trafficanda, Farm Fresh, Shoreland, Lund, Dutch Farms and Kemps. Eggs are packed in varying sizes of cartons (6-egg cartons, dozen egg cartons, 18-egg cartons) with Julian dates ranging from 136 to 225 and plant numbers 1026, 1413 and 1946. Dates and codes can be found stamped on the end of the egg carton. The plant number begins with the letter P and then the number. The Julian date follows the plant number, for example: P-1946 223.

There have been confirmed Salmonella enteritidis illnesses relating to the shell eggs and traceback investigations are ongoing. Wright County Egg is fully cooperating with FDA’s investigation by undertaking this voluntary recall. Our primary concern is keeping Salmonella out of the food supply and away from consumers. As a precautionary measure, Wright County Egg also has decided to divert its existing inventory of shell eggs to a breaker, where they will be pasteurized to kill any Salmonella bacteria present.

Consumers who believe they may have purchased these shell eggs should not eat them but should return them to the store where they were purchased for a full refund. This recall is of shell eggs only. Other egg products produced by Wright County Eggs are not affected. Consumers with questions should visit www.eggsafety.org Our farm strives to provide our customers with safe, high-quality eggs – that is our responsibility and our commitment."

Source: FDA
Image Source: FDA

Goya Frozen Fruit Linked to Typhoid Fever Outbreak

noreply@blogger.com (WOYP) — Thu, 12 Aug 2010 15:48:00 +0000

An outbreak of typhoid fever in the USA has been linked to a frozen tropical fruit product used to make smoothies. According to the CDC five of the seven confirmed cases drank milkshakes or smoothies made with frozen Mamey fruit pulp sold by Goya Foods Inc. of Secaucus, N.J. Of the seven cases, three are in California and four in Nevada. Five people have been hospitalized.

Mamey is a sweet grown mainly in Central and South America. It is also known as zapote or sapote. It is usually peeled and mashed to make pulp that is then frozen and sold.

The FDA reported that a sample from one package in Las Vegas tested positive for the bacteria that causes typhoid. Typhoid fever is a life-threatening illness caused by a type of bacteria called Salmonella typhi. Symptoms include a sustained fever as high as 103 to 104 degrees, along with headache. weakness, stomach pains or loss of appetite. Some patients have a rash of flat, rose-colored spots. It can be treated with antibiotics.

Goya has recalled packages of the pulp which was sold in the western USA. The recalled mamey pulp was sold in 14-ounce plastic packages in Alaska, Arizona, California, Colorado, Hawaii, New Mexico, Nevada, Oregon, Texas, Utah and Washington.
Also See: CDC - Typhoid Fever

More Information @: FDA

Photo Courtesy: FDA Product Labels

Kellogg agrees to Restrict Advertising

noreply@blogger.com (WOYP) — Sat, 05 Jun 2010 17:46:00 +0000

An investigation by the FTC into some of Kellogg's advertising claims about the health benefits of its Rice Krispies cereal has led to a settlement between the two parties. Kellogg's has agreed to advertising restrictions regarding the following statement on the cereal box which says:

now helps support your child’s immunity; has been improved to include antioxidants and nutrients that your family needs to help them stay healthy

The FTC s taking action against Kellogg at a time when public health researchers are intensifying their challenges to the marketing of sugary foods. They noted that:

We expect more from a great American company than making dubious claims — not once, but twice — that its cereals improve children’s health.

The new order bars Kellogg's from making any claims about any health benefit of any food unless the claims are backed by scientific evidence and not misleading.

Kellogg responded by noting that the company had a long history of responsible advertising.

Cadmium found on McDonald's 'Shrek' Glasses

noreply@blogger.com (WOYP) — Fri, 04 Jun 2010 17:40:00 +0000

Over 12 million glasses that were sold by McDonald's to promote the movie Shrek Forever After. This recalls follows a warning by the Consumer Product Safety Commission that they contain cadmium, a toxic metal. These glasses were sold only by the burger chain between May and June. The 16oz glasses were sold for $2.00 each and have a Shrek character painted on them.

Interestingly, the recall originated with an anonymous tip by an alert customer last week who told Rep. Jackie Speier (D) of California that the glasses contained cadmium. CPSC was contacted and the glasses were sent for testing. Speier has called for tougher safety standards for children's products.

Representative Speier noted:

Our children’s health should not depend on the consciences of anonymous sources. Although McDonald’s did the right thing by recalling these products, we need stronger testing standards to ensure that all children’s products are proven safe before they hit the shelves.

McDonald's notes that the glasses met federal safety standards during laboratory testing but they initiated this recall

in light of the CPSC's evolving assessment of standards for cadmium in consumer products

So far, no injuries from this product have been reported. For more information, consumers are encouraged to contact McDonald’s at (800) 244-6227 between 9 - 5CT Monday through Friday.

Lettuce Recall Due to EColi Contamination

noreply@blogger.com (WOYP) — Fri, 07 May 2010 14:44:00 +0000

A lettuce recall has been announced in 23 states and the District of Columbia apparently due to an outbreak of E. coli that has sickened at least 19 people. Three of them have life-threatening symptoms.

Local health departments in Ohio, Michigan, and NY noted that it is college students at the University of Michigan in Ann Arbor, Ohio State in Columbus and Daemen College in Amherst, N.Y., that are among those affected.

On Thursday, the FDA noted that 12 people were in hospital and the federal Centers for Disease Control and Prevention believed that another 10 cases were suspected to be linked to the outbreak.

In a press release, the FDA observed:

Multiple lines of evidence have implicated shredded romaine lettuce from one processing facility.

The lettuce came from Freshway Foods of Sidney, Ohio. They announced that they had initiated a voluntary recall of romaine lettuce sold under the Freshway and Imperial Sysco brands as they were believed to have a link to this E. coli outbreak. Freshway Foods said the lettuce was sold to wholesalers, food service outlets, in-store salad bars and delis.

Further, the FDA investigation is focusing on on lettuce being grown in Arizona as a possible source of this outbreak. E. coli infection can cause mild diarrhea or more severe complications, including kidney damage. The three patients with life-threatening symptoms were diagnosed with hemolytic uremic syndrome, which can cause bleeding in the brain or kidneys. The most common strain of E. coli found in U.S. patients is E. coli O157. The CDC said the strain linked to the lettuce, E. coli 0145, is more difficult to identify and may go unreported.

The recalled lettuce has a best if used by date of May 12 or earlier. The recall also affects "grab and go" salads sold at Kroger, Giant Eagle, Ingles Markets and Marsh grocery stores. The lettuce was sold in Alabama, Connecticut, the District of Columbia, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Missouri, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Virginia, West Virginia and Wisconsin.

Only last year, the House passed a bill last year giving the FDA enhanced authority to police food production. However, the Senate has not as yet acted on it.

In a statement yesterday, Freshway Foods said that:

an extensive FDA investigation

of Freshway Foods' facility in Sidney has not uncovered any contamination at the plant. Consumers with questions can call the company at 888-361-7106 on weekdays (8 a.m. to 5 p.m. EDT) or visit its website for updates (www.freshwayfoods.com). The company's press release is @ News.

Also see:
FDA Press Release
CDC Investigation Announcement

Undeclared Sulfites in "Nut Tree Health Mix"

noreply@blogger.com (WOYP) — Mon, 19 Apr 2010 19:16:00 +0000

The New York State Agriculture Commissioner has alerted consumers that Green Land, 212-03 48th Avenue, Oakland Garden, New York 11364, is voluntarily recalling Nut Tree Health Mix. This is because undeclared sulfites are present in the product. Persons with sulfite sensitivity risk serious or life-threatening reactions if they consume this product.

The recalled product is packaged in 8oz, square plastic tubs and coded DATE: SEP 28 10 in black ink on the product label. It was distributed in the metropolitan New York area. The sulfite contamination was discovered during a routine sampling by New York State Department of Agriculture and Markets' food inspectors. An analysis by the New York State Food Laboratory personnel of this product subsequently revealed the product contained high levels of sulfites. This was not stated on the label.

The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock can also occur in sulfite sensitive individuals who consume 10 mg or more of sulfites. So far, no illness has reported to the FDA in connection with this product. Consumers are advised to return this product to place of purchase.

Whole Foods Recalls Frozen Whole Catch Yellow Fin Tuna Steaks

noreply@blogger.com (WOYP) — Thu, 08 Apr 2010 18:39:00 +0000

Elevated levels of histamine has led to a Whole Foods recall of its Whole Catch Yellow fin Tuna Steaks (frozen) with a best by date of Dec 5th, 2010. The product, sold in twelve ounce bags with Best by Date: exp 05 DEC 2010 with Lot Code: 4853309157A and displays the following UPC code: 0-99482-42078-9 Whole Catch Yellow fin Tuna Steaks (Frozen) 12 oz.

Whole Foods Market has removed the affected lot code from all store shelves. Product was distributed to 28 states plus the District of Columbia including Texas, Oklahoma, Louisiana, Illinois, Indiana, Kansas, Ohio, Wisconsin, Minnesota, Missouri, Michigan, Maryland, Virginia, Pennsylvania, Florida, Alabama, Georgia, Kentucky, South Carolina, Tennessee, North Carolina, Connecticut, Nebraska, New Jersey, New York, Maryland, Rhode Island, Maine and Washington, D.C.
Elevated histamine may result in symptoms that generally appear within minutes to an hour after eating the affected fish. It can produce an allergic reaction called scombroid poisoning when the fish is consumed. The most common symptoms of scombroid poisoning include tingling or burning sensation in the mouth, facial swelling, rash, hives and itchy skin, nausea, vomiting or diarrhea. However, each individual may experience symptoms differently. There have been two reported incidents by consumers.

Consumers can return it to the store for a full refund, or call the company @ 512-542-0656.

More Information@: FDA

Zatarain's Recalls Original Dirty Rice Mix Package: Unlabeled Wheat & Barley

noreply@blogger.com (WOYP) — Fri, 02 Apr 2010 18:18:00 +0000

Zatarain's has announced a voluntary recall of one of their products as it contains undeclared wheat and barley ingredients. People with wheat or barley allergies have the risk of serious and even life threatening allergic reactions if they consume this product.

Zatarain's Original Dirty Rice Mix, 8 oz. package with UPC Code 7142909535 and a "BEST BY" date of JAN 19 12H.This product was distributed to some grocery stores in Florida, Michigan and Virginia from February 15, 2010 onwards. The product is sold in 8 oz. boxes. Its date code is at the bottom of the package.This recall was initiated after it was discovered that the product was mispackaged. The ingredient statement on the package does not list wheat and barley as an ingredient. So far, no illnesses or allergic reactions have been reported..

Any grocery selling Zatarain's New Orleans Style Dirty Rice Mix packages have been asked to remove these products from their shelves immediately. Consumers should contact Zatarain's Consumer Affairs at 1-877-837-3796, weekdays from 9:30 AM to 5:00 PM ET. You will receive a replacement or full refund and instructions on what to do with the product.

More Information @: FDA

Nationwide Recall of Whole Black Pepper in H.D.W. FOODS Labeled Bags

noreply@blogger.com (WOYP) — Wed, 31 Mar 2010 17:31:00 +0000

Perfect Candy & Packaging Co is joining a recall of Whole Black Peppercorns. This product recall has been initiated due to the possibility of contamination with Salmonella

The product has an H.D.W. Foods Inc. label:

Whole Black Peppercorns, 2.0 oz Bags UPC# 080869654293

The pepper was distributed nationwide, and all retailers carrying this product are advised to remove it from the shelves. If you have purchased this product, kindly destroy it immediately. If you have any questions regarding the product, kindly contact customer service @ Perfect Candy & Packaging Co at 610-373-3253.

For more information on FDA’s ongoing investigation: FDA

Modern Products recalls Seasonings: Possible Salmonella Contamination

noreply@blogger.com (WOYP) — Sun, 28 Mar 2010 17:03:00 +0000

Modern Products, Inc. is initiating a recall of products manufactured with HVP (Hydrolyzed Vegetable Protein). This ingredient is potentially contaminated with Salmonella. The HVP comes from Basic Food Flavors (Las Vegas, Nevada).

To date, no illnesses have been associated with any Modern Products seasonings. In addition, random samples covering all HVP batches of concern were sent to an independent laboratory for testing and all results came back negative, but to be safe, FDA's recommendation to recall product is being followed.

The recalled products were sold nation wide via retail stores. Products recalled include:

UPC Number - Product Description - Code Dates/Lot #

0-75820-00000-4 Spike Original Magic!, 3 oz. 9J19, 9J20, 9K12, 9K13, 9K16, 9K30, 9L16, 9L17, 9L28, 9L29, 10B10, 10B11, 10B12, 10B15, 10B25, 10B26

0-75820-20408-2 Spike Seasoning, 7 oz. 9J21, 9L01, 9L17, 9L28, 9L29, 10B15, 10B18

0-75820-20616-1 Spike Seasoning, 14 oz. 9L03, 9L17, 9L21, 9L30, 10A12, 10A13

0-75820-30030-2 Spike Seasoning, 5 lb. bulk 9K05, 9K09, 9K10, 9K16, 9K17, 9K30, 9L18, 9L21, 10A18, 10B17, 10B18, 10B19

0-75820-00002-8 Spike Vegit Magic!, 2 oz. 9K02, 9L16, 10A19, 10B12

0-75820-20806-6 Vegit Seasoning, 4 oz. 10B11

0-75820-21012-0 Vegit Seasoning, 8 oz. 9L30, 10A12

0-75820-00001-1 Spike Vege-Sal Magic!, 4 oz. 9K02, 9K03, 9L29

0-75820-15410-3 Vege-Sal Seasoning, 10 oz. 9J29, 9L09, 9L29, 10B11, 10B18

0-75820-15222-2 Vege-Sal Seasoning, 20 oz. 9K17, 9K19, 10A13

0-75820-00005-9 Spike Hot ‘n Spicy Magic!, 2.5 oz. 10A19, 10B15

0-75820-00003-5 Spike Tenderizer Magic!, 3-3/4 oz. 9K03, 10B25

0-75820-00008-0 Spike Onion Magic!, 2-1/2 oz. 10B15

0-75820-17804-8 Hauser Vegetable Broth, 4 oz. 9L08, 10B11

0-75820-18008-9 Hauser Vegetable Broth, 8 oz. 9K09, 9K10, 10A14

The codes can be found along the base of the bottles/jars. Cartons/boxes will have the code embossed along the top of the package.

About Salmonella: Consuming products contaminated with Salmonella can cause serious and even fatal infections in persons who have a weak immune system. Young children, frail, and elderly people are particularly vulnerable. Healthy persons infected with Salmonella usually get fever, diarrhea, nausea, vomiting and abdominal pain. Salmonella can also result more severe illnesses like arterial infections, infected aneurysms, endocarditis and arthritis.

For further information, contact:
Modern Products, Inc.
Tel 262-242-2400
Email modernfearn@aol.com

Further Information via: FDA Recall Alert

Soft Drinks & Pancreatic Cancer

noreply@blogger.com (WOYP) — Mon, 08 Feb 2010 15:58:00 +0000

Soft drinks are linked with a higher risk of pancreatic cancer. We can't speculate too much on the mechanism because this is an observational study, but the increased risk may be working through effects of the hormone insulin.

Noel Mueller, lead author of study February issue of Cancer Epidemiology, Biomarkers & Prevention.

Mueller's research notes that people who consume over two soft drinks per week are likely to double their risk of the deadly pancreatic cancer. The study was a collaboration between the University of Minnesota and National University of Singapore. It involved over 60,000 middle-aged or older Chinese Singaporeans. Researchers calculated how much juice and soda the participants drank on average and followed them for 14 years to see how many developed cancer of the pancreas. Based on this long-term approach, the research revealed that people who drank two or more sodas a week were 87 percent more likely to develop this cancer than those who didn't consume any soda.

The research also found no link between juice consumption and cancer risk. Previous research in U.S. and European populations has suggested an association between sweetened sodas and pancreatic cancer. This is the first study that has examined this association in an Asian population, though researchers believe that the findings will likely prove true for Western populations due to similarity of lifestyle and diet.

Type 2 diabetes, a disorder of blood sugar levels and insulin under-activity, has also been linked in studies to pancreatic cancer. Researchers suggest that high levels of blood sugar are associated with drinking soda and an associated increase in insulin levels. This increase prompts pancreatic cells to divide abnormally. Sugar-sweetened soft drinks can lead to weight gain, obesity, and eventually diabetes. Both obesity and diabetes are associated with higher risk of pancreatic cancer, one of the leading causes of cancer death in the US.

Some researches however have observed that the report should not cause undue alarm as adult soda drinkers are likely to engage in other lifestyle habits, including smoking, which may also contribute to the elevated risk.

The soft drink industry on the other hand disputes the findings. Richard Adamson, a consultant to the American Beverage Association and former scientific director of the NCI said:

The [study] authors are skipping several steps in trying to connect soft drinks with pancreatic cancer, including an allegation regarding an increase in insulin production. The fact remains that soft drinks do not cause cancer, nor do any authoritative bodies, such as NCI, name soft drinks as a risk factor for pancreatic cancer. You can be a healthy person and enjoy soft drinks. The key to a healthy lifestyle is balance -- eating a variety of foods and beverages in moderation along with getting regular physical activity.

All in all, it might be wise to consider a more cautious view of the situation - soda is not a food and does not belong to any food group. Eat healthy, and remember that moderation is the best mantra for all consumption and lifestyle related issue.

Fertility Alert over PBDEs found in Household Consumer Products

noreply@blogger.com (WOYP) — Wed, 27 Jan 2010 14:54:00 +0000

Many household consumer products contain flame-retardant chemicals that research suggests reduces fertility in women. This comes as a part of a new research which reinforces previous studies on this topic. Papers published in the last two years have repeatedly suggested that the chemicals, polybrominated diphenyl ethers or PBDEs, affect human health.

PBDEs have been used as flame retardants in the USA for almost four decades. They are common in foam furniture, electronics, fabrics, carpets and plastics. While these chemicals are slowly being phased out, they are still found in products that were made prior 2004. Some of these chemicals have already been banned in California, but ironically Californians are expected to have higher exposures to them because of the state's strict flammability laws.

The authors of the study from UC Berkely noted that most of the previous research on the chemicals has been in animals. However a 2008 study linked the chemicals to disrupted thyroid levels in men. Further, a study published earlier this month tied PBDE exposure in pregnancy to neurodevelopmental delays in young children.

Dr. Hugh Taylor, an expert at Yale University not involved in this study says:

These are association studies. You can't show cause and effect. But we have cause-and-effect studies in animals, and we have association studies in humans. I think that is fairly convincing.

In the new study, published in the journal Environmental Health Perspectives, researchers measured PBDE levels in blood samples from 223 pregnant women who were mainly Mexican immigrants living in an agricultural community. They were asked to remember how long they had been trying to become pregnant i.e. being sexually active without using birth control.

The research found that the women with the highest concentrations of PBDEs took a longer time to get pregnant. More alarming was the discovery that every 10 fold increase in the blood concentration of PBDEs led to a 30% decrease in pregnancy each month.

Previous studies had shown that 97% of Americans have trace levels of PBDEs in their blood, which may have come from some foods like dairy products, meat and fish, though household products are viewed as the primary source of exposure.

Environmental Protection Agency and the two largest manufacturers of one type of PBDE agreed to phase out the chemical only last month. The EPA banned two of the three mixtures of PBDE developed for commercial use as flame retardants in 2005, and a 3rd is to be phased out of production in 2013.

The study's lead author, Kim Harley, adjunct assistant professor of maternal and child health and associate director of the Center for Children's Environmental Health Research at Berkeley's School of Public Health observed:

The good news is these chemicals have or are being phased out. The bad news is their legacy will continue because of their presence in a lot of items in our homes.

But PBDEs, like many other hazardous chemicals before them, will be in the environment a long after they are banned for use.

Nipro Med Corp recalls 2 million medical needles in U.S.

noreply@blogger.com (WOYP) — Wed, 27 Jan 2010 03:33:00 +0000

A subsidiary of the Japanese company Nipro Corp, Nipro Medical Corporation, Miami FL, is initiating 2 nationwide recalls of syringes manufactured by them. The first is of all GlucoPro Insulin Syringes and was initiated on January 21, 2010. According to the FDA, these syringes may have needles that detach from the syringe. If the needle becomes detached from the syringe during use, it can become stuck in the insulin vial, push back into the syringe, or remain in the skin after injection.

This recall includes all product codes and lot numbers with expiration dates before 2011-11 (Nov 1, 2011):
Product Code Lot # Expiry date
JD+01U3008-5C A08022 2011-11
JD+01U3013-5C A08013 2011-06
JD+01U3013-5C A08017 2011-08
JD+01U3108-5C A08013 2011-06
JD+01U3108-5C A08017 2011-08
JD+03U3008-5C C08022 2011-11
JD+03U3013-5C C08013 2011-06
JD+03U3013-5C C08017 2011-08
JD+03U3108-5C C08013 2011-06
JD+03U3108-5C C08017 2011-08
JD+05U3008-5C B08022 2011-11
JD+05U3013-5C B08013 2011-06
JD+05U3013-5C B08017 2011-08
JD+05U3108-5C B08013 2011-06
JD+05U3108-5C B08017 2011-08

The second is a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation. This includes 2 million Huber infusion set needles distributed in the United States. An October 2009 inspections of Nipro facilities by the FDA found problems with the needles that could allow pieces of the port's silicone core to become dislodged. The inspections found around 60-72% of Nipro's needles tested had this problem.

The needles are used for special medical purposes including accessing ports implanted under the skin of chronically ill patients for repeated access to veins, withdrawing blood, and injecting medicines. These needles should be designed to penetrate the port without cutting and dislodging any silicone cores (or slivers) from the ports into which they are inserted. The needles were distributed by privately held Exel International from Los Angeles. As of now, no injuries have been reported, FDA officials noted that they were concerned a piece of silicone could enter a patient's bloodstream.

Recalled needles were manufactured from January 2007 to August 2009. Units subject to recall have a lot number that begins with “07,” “08,” “09,” and one of the following product codes or catalog numbers:

Exel/Exelint Huber Needles Product Codes/Catalog Numbers:
26901
26902
26904
26906
26907
26908
26909
26911
26921
26922
26923
26924
26925

Exel/Exelint Huber Infusion Sets Product Codes/Catalog Numbers With/Injection Site:
27940R
27941R
27944R
27945R
27946R
27948R
27949R
27950R

Without/Injection Site Product Codes/Catalog Numbers:
27954R
27955R
27958R
27959R
Exel/Exelint “SecureTouch +” Safety Huber Sets Product Codes/Catalog Numbers:
37854S
37855S
37858S

Hospitals, clinics and patients who have needles from these lists should immediately stop using these affected products and return any unused products to Exelint International Corporation. The FDA has issued a letter to manufacturers of other Huber needles to address design and manufacturing concerns.

Further Details @ FDA.gov

Parker's Farm Recall Extended to their Products sold at Wisconsin Cheeseman®

noreply@blogger.com (WOYP) — Sat, 23 Jan 2010 04:44:00 +0000

The Wisconsin Cheeseman® has recalls Cheese Logs/Cheese Balls products in conjunction with the voluntary recall initiated by Parkers Farm, Inc. on January 15, 2010.

Parkers Farm, Inc., located in Coon Rapids, Minnesota, believes some of its food items have the potential to be contaminated with Listeria monocytogenes bacteria. The recall was a result of a sampling done by the state of Wisconsin and the state of Minnesota.

Nine of the recalled products are cheese logs/cheese balls purchased from Parkers Farm, Inc. and then distributed by The Wisconsin Cheeseman®. These products bear the Parkers Farm logo. None of the other recalled products at Parkers Farm, Inc. was purchased or distributed by The Wisconsin Cheeseman®.

The Wisconsin Cheeseman® Food Gifts Impacted by Recall:
Sausage 'N Cheese Logs – Gift #11
Cheese Logs & Cutting Board – Gift #87
Smorgasbord – Gift #325
Cheese Log Trio – Gift #365
Cheese Logs – Gift #411
Cheese Ball Trio – Gift #441
Cheese Logs – Gift #509
Snacker Pack – Gift #751
Cheese Balls & Sausages – Gift #876

The FDA asks consumers who have any of these products in their possession to throw them out. Alternatively, the product can be returned to The Wisconsin Cheeseman® for a refund or replacement. Consumers who believe they may have become ill after consuming these products should immediately contact their health care provider.

Pandemic Flu & Vaccine Supply - A WHO Controversy

noreply@blogger.com (WOYP) — Wed, 20 Jan 2010 20:22:00 +0000

India today asked the WHO to explain reports that swine flu was a false pandemic. During a meeting of the WHO Executive Health Board, the Indian Union Health Secretary noted that news reports that the pandemic was false were adversely impacting the public health measures being undertaken in various nations. She also called for greater transparency on terms and conditions on which international vaccine manufacturers were supplying vaccines globally.

In response to this intervention by India, the WHO has agreed to formally write to National Focal Points in all countries clarifying the factual position about the H1N1 pandemic. This should quell all doubts that had been created by recent reports which have placed the organisation squarely and rather uncomfortably in the middle of this controversy.