Tag Archives: Food And Drug Administration

GMO labeling lies


AlterNet – I522 and Washington State

Zack Kaldveer, AlterNet

Here are the lies. And the facts. Please read, print, email, roll up and stuff into a bottle you launch into the sea . . . whatever it takes to spread the word that while $46 million may buy a lot of lies, it doesn’t change the facts.

1. Lie: Labeling genetically engineered foods (GMOs) will cost taxpayers millions of dollars a year.

Truth: Empirical  studies have concluded labeling would lead to no increases in prices. Since the European Union labeled GMOs in the 1990’s, there has been ” no resulting increase in grocery costs.”

Trader Joe’s, Clif Bar & Co. and Washington’s own PCC Natural Markets all  label their non-GMO product lines at no additional cost to consumers.

2. Lie: I-522 is full of arbitrary special interest exemptions that will just confuse consumers.

Truth: I-522 requires labeling for the GE foods that are most prevalent in the American diet – food on supermarket shelves. I-522’s exemptions are easy to explain and guided by common sense and the law:

  • Restaurants – Restaurants and bake sales are not required to list the ingredients in their products. Requiring labeling for GMOs would have required tracking all the ingredients in restaurant meals, and since no other laws require that, it didn’t make sense for this one to.
  • Meat, cheese, dairy and eggs from animals – These will be labeled if they come from genetically engineered animals. However, they are exempt if the animals ate genetically engineered feed but are not themselves genetically engineered. This exemption is common all around the world. It didn’t make sense for Washington’s law to be stricter than international standards.
  • Alcohol – Alcohol labeling is regulated under different laws than food at both the federal and state levels. Because of the single-subject law that requires initiatives to apply to only one subject, alcohol couldn’t be included.

3. Lie: Consumers don’t need labels to avoid GMOs. All they need to do is buy certified organic products.

Truth: Food companies routinely and intentionally mislead consumers by labeling products “natural” in order to attract health-conscious consumers. Because the U.S. Food & Drug Administration (FDA) does not prohibit the use of the word “natural” on products containing GMOs, most consumers are fooled by this label. According to a recent  poll by the Hartman group, 61 percent of respondents erroneously believed that the use of the word “natural” implies or suggests the absence of GMOs, versus 63 percent who correctly believed that the label “organic” means that a product is GMO-free. Food companies should be required, as they are in some 60 other countries, to clearly state that a product contains GMOs. If companies truly believe their GMO ingredients are perfectly safe, why spend millions to keep from having to label them?

4. Lie: Washington will be the only state in the nation to label GMOs, unfairly hurting farmers and the state’s multi-billion agricultural industry.  

Truth: Washington won’t be the only state labeling GE foods.  Connecticut, Maine and Alaska have passed labeling laws and dozens of other states are considering identical proposals. Besides, 64 countries already require labeling, so many farmers are already used to labeling for exports. In fact, many Washington farmers support labeling because they believe that growing GMO crops destroys healthy soil, and because they sell crops to overseas markets that either require labels on GMO crops, or have banned them completely. These countries are increasingly concerned about U.S. non-GMO crops, such as wheat, that could potentially be  contaminated by  cross-pollination with GMO crops.

Update: Stop GMO salmon


The FDA must require labeling of genetically modified salmon.
Submit your comment asking the FDA to require clear labels on GMO salmon, or better yet, ban GMO fish altogether.  


Earlier this year we let you know about the Food and Drug Administration’s impending approval of a genetically modified (GMO) strain of salmon. Over 54,000 CREDO Action members responded by telling the FDA not to approve the fish.

There are some signs that our pressure is working. At the public hearing in September several members of the advisory committee criticized the poor science submitted by AquaBounty, the company engineering the fish, and called for more rigorous scientific review before moving forward with the approval process.1

While the committee has not yet issued a recommendation on whether to approve the salmon, the FDA has opened a public comment period on labeling requirements should the organism be brought to market. We still firmly believe that AquaBounty’s application should be rejected, but we need to fight this battle on all fronts.

We have until November 22 to let the FDA know that it should not approve GMO salmon, but if it does, to enact strict labeling requirements — so consumers can at the very least make educated decisions about what they eat.

People who know anything about this salmon have good reason to be afraid. The fish is modified with genes from another species — the eelpout — so that it can grow twice as fast as normal.2

Because the FDA is reviewing the salmon application under its rules for animal drugs, there is little focus on the potential dangers of human consumption. Additionally, the FDA has not conducted any of its own research and is instead relying on information provided by AquaBounty, a company that has a financial incentive to downplay potential dangers.

There are also serious concerns about the environmental impact of the fish. Studies show that if just a few GMO salmon escaped into the wild, they could eradicate the wild Atlantic salmon population in less than 40 fish generations.3

Clearly, the FDA shouldn’t allow the fish to be produced in the first place. But if it does, the FDA should require that it be clearly labeled so we can decide on our own to keep it off our dinner plates.

The November 22 deadline is approaching. Submit your public comment today telling the FDA to enact clear labeling requirements for GMO salmon, or better yet, keep it off the market altogether.

Adam Klaus, Campaign Manager
CREDO Action from Working Assets

USDA-FSIS Recall Cases ~~ Nov 2013


USDA logo
USDA logo (Photo credit: Wikipedia)

Updated information is now available. An updated list of retail consignees has been posted for recall 065-2013, California Firm Recalls Grilled Chicken Salad Products Due To Possible E. Coli O157:H7 Contamination (Nov 10, 2013).

Utah Firm Recalls Fully-Cooked-Not-Shelf-Stable, Ready-To-Eat Pork Roast Products Produced Under The Wrong Haccp Plan And For Mislabeling
Creminelli Fine Meats, LLC, a Salt Lake City, Utah, establishment, is recalling 31 pieces (approximately 101 pounds) of fully-cooked-not-shelf-stable,  ready-to-eat pork roast products because they were produced under the wrong Hazard Analysis and Critical Control Point (HACCP) plan and for mislabeling

Wisconsin Firm Recalls Frozen Chicken Products Due To Misbranding and Undeclared Allergen
Intevation Food Group, LLC, a Plover, Wis., establishment, is recalling approximately 156,924 pounds of frozen chicken fettuccine Alfredo products because of misbranding and an undeclared allergen. The products contain egg, a known allergen, which is not declared on the product label

Updated information is now available. An updated list of retail consignees has been posted for recall [066-2013], [Texas Firm Recalls Various Raw Poultry Products Produced Without the Benefit of Inspection], (November 13, 2013).

Texas Firm Recalls Various Raw Poultry Products Produced Without the Benefit of Inspection
Fran’s Fryers, a Milford, Texas, establishment, is recalling approximately 251 pounds of various raw poultry products because they were produced without the benefit of federal inspection.

Updated information is now available. An updated list of retail consignees has been posted for recall 065-2013California Firm Recalls Grilled Chicken Salad Products Due to Possible E. Coli 0157:H7 Contamination, November 10, 2013

Updated information is now available. An updated list of retail consignees has been posted for recall 059-2013 (October 22, 2013),recall 059-2013-expansion (October 26, 2013) and recall 059-2013-expansion-2 (November 4, 2013), Kansas Firm Recalls Chicken, Ham And Beef Products Due To Potential Listeria Monocytogenes Contamination.

Updated information is now available. An updated list of retail consignees has been posted for recall [059-2013], [California Firm Recalls Grilled Chicken Salad Products Due To Possible E. Coli O157:H7 Contamination], (November 10, 2013).

California Firm Recalls Grilled Chicken Salad Products Due To Possible E. Coli O157:H7 Contamination From this morning
Glass Onion Catering, a Richmond, Calif. establishment, is recalling approximately 181,620 pounds of ready-to-eat salads and sandwich wrap products with fully-cooked chicken and ham that may be contaminated with E. coli O157:H7.

Recall Notification Report 064-2013
Wycen Foods Inc., a San Leandro, Calif., establishment is recalling approximately 809 pounds of Chinese style chicken sausages, a dried snack food, because they are misbranded and contain monosodium glutamate (MSG), which is not declared on the label.

Kansas Firm Recalls Chicken, Ham and Beef Products Due To Potential Listeria Monocytogenes Contamination 
Reser’s Fine Foods, a Topeka, Kan. establishment, is expanding its recall of chicken, ham and beef products to include all products produced between Oct. 10 and Oct. 25, 2013. The company previously expanded its recall on Oct. 26, 2013,to include product produced between Sept. 5 and Oct. 9, 2013. This is in addition to the 22,800 pounds of product recalled on Oct. 22, 2013.

FDA Alerts & Recalls ~~ Nov 2013


English: Logo of the .
English: Logo of the . (Photo credit: Wikipedia)
11/27/2013 04:38 PM EST
Flat Creek Farm and Dairy of Swainsboro, GA has recalled 200 pounds of Heavenly Blue cheese, because of potential contamination. As of November 27, 2013 at 11:00am, according to Flat Creek records, all of the purchasers have been notified and more than 90% of the product has been collected or destroyed.

Zip International Group LLC Recalls Herring Fillet in Oil Due to Potential Health Risk

11/27/2013 10:07 AM EST
ZIP INTERNATIONAL GROUP LLC, 160 Raritan Center Parkway #6, Edison, NJ 08837, is recalling herring fillet in oil (FOSFOREL, ATLANTIKA) 400 gram in plastic packaging due to Listeria contamination.

CLR Medicals International Inc. Issues Nationwide Recall of Viscoelastic Products

11/25/2013 07:39 PM EST
CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspectional findings of deficiencies in the Quality System regulations for Medical Device Manufacturers, 21 Code of Federal Regulation (CFR) Part 820 and lack of Premarket Approval (PMA) for devices sold or distributed in domestic commerce. The Viscoelastic products, intended for human and animal use, have been determined to be a public health concern due to distribution in the US without FDA approval, which evaluates the safety and efficacy of the product, and violations of the QSR regulations related to sterility, and biocompatibility that may result in the release of contaminated products.

Jayone Food Issues Voluntary Alert on Undeclared Peanuts in Dried Seaweed Salad

11/23/2013 09:18 PM EST
Jayone Foods, inc. of Paramount, CA is voluntarily recalling All date codes of Trader Joe’s Dried Seaweed Salad with Spicy Dressing (SKU 97677), because it may contain traces of peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

Recall expanded to include: Raspberry Lemonade OxyELITE Pro Super Thermo Powder

11/19/2013 08:44 PM EST
USPlabs LLC, Dallas, TX is voluntarily conducting a national recall of all lots and sizes of the OxyElite Pro dietary supplement products listed below. These products contain Aegeline, a synthesized version of a natural extract from the Bael tree.
11/19/2013 03:49 PM EST
Blount Fine Foods of Fall River, MA is recalling a single lot code of Wegman’s branded refrigerated New England Clam Chowder in 16 ounce retail cup pack size because of undeclared crab allergen. People who have an allergy or severe sensitivity to crab run the risk of suffering serious or life-threatening reactions if they consume this product.
11/18/2013 01:00 PM EST
FDA used new enforcement tools provided by the FDA Food Safety Modernization Act to act quickly in the face of a potential danger to public health.
 Following FDA actions, USPLabs on Nov. 9, 2013 recalled certain OxyElite Pro dietary supplements linked to dozens of cases of acute liver failure and hepatitis, including one death and illnesses so severe that several patients required liver transplants. Additionally, FDA will oversee the destruction of warehouse stocks of the supplement, with a retail value of about $22 million.
While FDA’s investigation is still ongoing, the agency continues to warn consumers to avoid using OxyElite Pro and VERSA-1. Both products contain a new dietary ingredient for which the company did not provide evidence of safety.
11/15/2013 08:59 PM EST
La Boulange Cafe & Bakery voluntarily initiated a product recall of 75 Soft Caramel Jams in 8.4 oz. jars with lot number 822713 as a precautionary measure. This product was sold exclusively in 20 La Boulange Café & Bakery stores in the San Francisco Bay Area.
11/15/2013 03:18 PM EST
S&M Enterprise of Bayonne, NJ is recalling all lots of Fruit of Wolfberry in 12 oz plastic bag packages. People who have allergies to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products.
11/14/2013 11:45 PM EST
Crunch Pak of Cashmere, Washington is voluntarily recalling 5,471 cases of Crunch Pak Apple Slices due to a possible health risk from Listeria monocytogenes.
11/07/2013 10:50 AM EST
Bailey’s Choice LLC. in Waleska, GA is recalling its 5 oz. packages of chicken treats because they have the potential to be contaminated with Salmonella, 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 (which may be bloody), 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 (i.e., infected aneurysms), endocarditis and arthritis.
11/13/2013 04:52 PM EST
3 Fellers LLC is voluntarily initiating a product recall of 3 Fellers Chocolate Cream Pies with the UPC# 891796002732 as a precautionary measure. The recall was initiated after it was discovered by the company that the product may contain undeclared almonds.
11/12/2013 05:13 PM EST
Whole Foods Market’s Northern California region is recalling ready-to-eat Artichoke Wheatberry Salad and Southwest SooFoo®* Salad in response to a recall issued today by Glass Onion Catering. The salads are being recalled as a preventive measure because they have the potential to be contaminated with E. coli O157:h7, a bacteria that may cause illness.
11/08/2013 10:04 PM EST
Sequel Naturals Inc., dba “Vega,” announced today that it has taken the precautionary measure of voluntarily withdrawing a limited quantity of its Vega One Nutritional Shakes and Sports Performance Protein products due to finding trace amounts of chloramphenicol (CAP), a naturally occurring antibiotic. Chloramphenicol is a prescription drug commonly used to treat typhoid fever and eye infections around the world. It should only be used under medical supervision.
11/10/2013 08:27 PM EST
Athertone Foods, Inc. of Richmond, CA is voluntary recalling “Best Buy” dates 9-23-13 through 11-14-13 of ready to eat salads and wraps because they may be contaminated with Escherichia coli O157:H7 bacteria (E. coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools.
11/11/2013 01:43 PM EST
Palmer Candy Company of Sioux City, IA is recalling 102 cases of HyVee Chocolate Caramel Clusters and 90 cases HyVee Chocolate Covered Caramels because they may contain undeclared peanuts. People who have an allergy to peanuts run the risk of a serious or life-threatening allergic reaction if they consume these products.
11/09/2013 03:27 PM EST
Plum Organics is voluntarily recalling pouch products within its Baby Stage 2, Tots Mish Mash and Kids lines after discovering a manufacturing defect that may cause spoilage in some pouches. Recalled products can be identified by the “Best By” dates ranging from 08/05/14 to 12/08/14 and the letters “AT.”
11/05/2013 03:59 PM EST GOURMET EXPRESS, LLC VOLUNTARILY RECALLS 32 OUNCE PACKAGES OF “FUSIA CHICKEN LO MEIN” AND 21 OZ PACKAGES OF “BREMER 3 CHEESE CHICKEN” AND “BREMER GARLIC SHRIMP SKILLET MEALS DUE TO POSSIBLE UNDECLARED. People who have allergies to egg, run the risk of serious or life-threatening allergic reaction if they consume these products
11/04/2013 01:32 PM EST
October 30, 2013 – Garden-Fresh Foods is initiating an expansion to our voluntary recall on various ready-to-eat salads, slaw, and dip products sold under various brands and code dates (see attachment). The products included in the expanded recall were produced between the dates of September 5, 2013 through October 16, 2013.
11/05/2013 03:59 PM EST
GOURMET EXPRESS, LLC VOLUNTARILY RECALLS 32 OUNCE PACKAGES OF “FUSIA CHICKEN LO MEIN” AND 21 OZ PACKAGES OF “BREMER 3 CHEESE CHICKEN” AND “BREMER GARLIC SHRIMP SKILLET MEALS DUE TO POSSIBLE UNDECLARED. People who have allergies to egg, run the risk of serious or life-threatening allergic reaction if they consume these products.

Teens and Steroids: A Dangerous Combo

11/04/2013 11:00 AM EST Teens are particularly at risk for adverse effects associated with anabolic steroids—possible mood swings, aggressive behavior, heart and liver disease, shrinkage of the testes in males, and menstrual irregularities in women. Ali Mohamadi, M.D., a medical officer in the Food and Drug Administration’s Division of Metabolism and Endocrinology Products, warns teens and parents about the dangers of steroid use.

11/04/2013 01:32 PM EST
October 30, 2013 – Garden-Fresh Foods is initiating an expansion to our voluntary recall on various ready-to-eat salads, slaw, and dip products sold under various brands and code dates (see attachment). The products included in the expanded recall were produced between the dates of September 5, 2013 through October 16, 2013.
11/04/2013 01:07 PM EST
Reser’s Fine Foods, Inc. of Beaverton, Oregon is voluntarily expanding its October 22, 2013 recall of refrigerated ready-to-eat products because they may be contaminated with Listeria monocytogenes. Listeria is an organism which can cause serious and sometime fatal infections in young children, frail or elderly people and individuals with weakened immune systems.
11/04/2013 12:33 PM EST
Ghiringhelli Specialty Foods of Vallejo, California is voluntarily recalling one specific lot of Trader Giotto’s Caesar Salad (SKU 05161) with a “Use By 11/03” date, because it may not list wheat, soy and fish (anchovy) in the ingredients. People who have an allergy or severe sensitivity to wheat, soy and/or anchovy run the risk of serious or life-threatening allergic reaction if they consume these products.
11/01/2013 05:53 PM EDT
Following the Reser’s Fine Foods (“Reser’s”) recall where select Reser’s products were recalled due to the potential of being contaminated with Listeria monocytogenes, Dutch Treat Salads, LLC, of Zeeland, MI, is voluntarily recalling one product, Mexicali Dip, that contains one ingredient recalled by Reser’s.
11/01/2013 10:18 PM EDT
The Perrigo Company (NYSE: PRGO; TASE) announced today that it has initiated a voluntary, nationwide product recall to the retail level of 18 batches of its acetaminophen infant suspension liquid, 160 mg/5 mL, sold in 2 oz. and 4 oz. bottles with syringes in a box under the store brand products listed below. The recall is being initiated because of the remote potential that a small number of packages might contain an oral dosing syringe without dose markings.
11/01/2013 04:07 PM EDT
Winn-Dixie today announced an immediate recall in all Winn-Dixie stores of the Taylor Farms Broccoli Crunch Salad sold in the full-service case in the deli department. According to the U.S. Food and Drug Administration, the reason for the recall is the potential that the product may be contaminated with Listeria monocytogenes. The recall is part of a larger recall issued by Taylor Farms Tennessee, Inc. and Taylor Farms Maryland, Inc. as a result of a recall of Reser’s Fine Food Inc. products.
11/01/2013 04:10 PM EDT
Winn-Dixie today announced an immediate recall of the Taylor Farms Spinach Antipasta Salad in all Winn-Dixie stores. This recall is an expansion of an earlier recall announced by Reser’s Fine Foods, Inc.

FDA Alerts & Recalls


11/01/2013 02:12 PM EDT
The recent expansion of the Reser’s Fine Foods product recall for potential Listeria monocytogenes contamination has impacted select prepared foods offerings sold at Giant Eagle, Inc. locations in Pennsylvania, Ohio, Maryland and West Virginia. As a result, Giant Eagle has implemented a voluntary recall of Diced Summer Slaw, Diced Summer Salad and several Grab and Go combo meals that may include Diced Summer Slaw.

 

 

The Perrigo Company announced that it has initiated a voluntary, nationwide product recall to the retail level of 18 batches of its acetaminophen infant suspension liquid, 160 mg/5 mL, sold in 2 oz. and 4 oz. bottles with syringes in a box under store brand products including Babies R Us, Care One and more  (refer to the Firm Press Release for full list of affected brand names and products).

English: Logo of the .
English: Logo of the . (Photo credit: Wikipedia)
10/31/2013 06:36 PM EDT: On September 16, 2013 PENTAX Medical Company initiated a voluntary nationwide recall of 76 PENTAX Gas/ Water Valves, model OF-B194. The valves were offered as a separate purchase for use with PENTAX GI Video Endoscopes (90i/90k series and i10/k10 series).
10/31/2013 09:11 PM EDT
World Class Distribution of Fontana, California is voluntarily recalling one specific lot of Trader Joes Southwest Salad (SKU 56077) with a Use by Date11/2/13, because it may not list soy in the ingredients. 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. No illnesses have been reported to date.

Updated information Maryland Firm Recalls Broccoli Salad Kits for Possible Listeria Contamination (Oct 25, 2013) / Maryland and Texas Firms Recall Broccoli Salad Products with Dressing for Possible Listeria Contamination (Oct 29, 2013).

 10/26/2013 08:47 AM EDT
Kraft Foods Group is voluntarily recalling some varieties of Kraft and Polly-O String Cheese and String Cheese Twists products. These products may spoil before their “Best When Used By” code dates, leading to product discoloration.
10/26/2013 09:29 PM EDT
Reser’s Fine Foods of Beaverton, Oregon is voluntarily expanding its October 22, 2013 recall of refrigerated ready-to-eat products because they may be contaminated with Listeria monocytogenes. Listeria is an organism which can cause serious and sometime fatal infections in young children, frail or elderly people and individuals with weakened immune systems
10/07/2013 08:35 AM EDT
Orange County Produce, LLC (“OC Produce”) is voluntarily working with the Food and Drug Administration (“FDA”) and California Department of Public Health (“CDPH”) to coordinate a recall of fresh red and green Bell Peppers for potential contamination with Salmonella. The FDA has advised that a random sample of OC Produce Bell peppers has tested positive for Salmonella.
10/01/2013 05:45 PM EDT
Mandy Star Trading Inc., located at 349 Maujer Street Brooklyn NY 11206 is recalling “Good Taste” brand Plum, because it contains undeclared sulfites and unallowed E124 (Acid Red 18) dye. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening allergic-like reactions if they consume this product.
10/04/2013 07:42 PM EDT
Atossa Genetics Inc. (NASDAQ: ATOS) initiated a voluntary recall to remove the ForeCYTE Breast Health Test and the Mammary Aspiration Specimen Cytology Test (MASCT) device from the market. This voluntary recall includes the MASCT System Kit and Patient Sample Kit.
10/04/2013 07:39 PM EDT
Hospira, Inc.(NYSE: HSP), announced today it has initiated a voluntary nationwide recall of one lot of 1% Lidocaine HCI Injection, USP, 10 mg/mL, 20 mL Multiple-dose Fliptop Vial, NDC 0409-4276-01 Lot 25-090-DK (the lot number may be followed by 01 or 02).
10/03/2013 08:21 PM EDT
OnTime Distribution Inc. of Brooklyn, NY, is voluntarily recalling PRAN brand Spice Powder TURMERIC because it was found to contain high levels of lead that could cause health problems to consumers, particularly infants, small children, and pregnant women if consumed. Recent analysis of the product found that it contained lead levels as high as 28 and 42 parts per million (ppm).
10/04/2013 05:29 PM EDT
On August 27, 2013, H&H Medical Corporation initiated a nationwide recall of 6,619 units of the H&H Emergency Cricothyrotomy Kit. The product has been found to show the potential for a defective cuff balloon on the provided endotracheal airway.
10/08/2013 10:37 AM EDT
Today Dräger issued a statement regarding its voluntary recall on specific Fabius anesthesia machines. Dräger initiated this voluntary action in August of 2013 as a result of an internal investigation into devices that did not pass the high voltage test portion of the final production test.
10/15/2013 08:55 AM EDT
Yoder’s Country Market, is recalling custom gift boxes distributed in December 2012 because they may contain 11 oz. bags of honey roasted peanuts which contain undeclared milk and wheat. People who have allergies to milk or wheat run the risk of serious or life-threatening allergic reaction if they consume the honey roasted peanuts. No other components of the gift boxes are affected.
10/11/2013 04:36 PM EDT
Barrel O’ Fun Snack Foods Co. of Perham, MN is recalling one specific lot of Safeway Snack Artist BBQ Potato Chips (UPC 21130-29106) because they contain undeclared milk. People with an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reactions if they consume this product.
10/07/2013 02:34 PM EDT
Turkey Hill Dairy of Conestoga, Pa., is recalling specific packages of 1.5 qt. (48 oz./1.42L) of Fudge Ripple Premium Ice Cream and 1 Pint (16 oz./473 ml) packages of Chocolate Peanut Butter Cup Premium Ice Cream, and Moose Tracks Stuff’d Frozen Dairy Dessert due to the possibility that some packages may contain metal shavings.
10/15/2013 04:39 PM EDT
B. Braun Medical Inc. (B.Braun) is voluntarily recalling one lot of 1g Cefepime for Injection USP and Dextrose Injection USP (Lot H3A744, catalog 3193-11) to the consumer level. The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample unit
10/02/2013 10:25 AM EDT
Hospira, Inc. (NYSE: HSP), announced today it initiated a voluntary nationwide recall of one lot of Metoclopramide Injection, USP, 10 mg/2 mL (5 mg/mL), NDC 0409-3414-01, Lot 28-104-DK and two lots of Ondansetron Injection, USP, 4 mg/2 mL, (2 mg/mL), NDC 0409-4755-03, Lots 29-484-DK and 29-510-DK. This action is due to a confirmed vial defect where glass particulate matter (glass strands) were identified as being affixed to the inside of the vial walls. There is potential for the glass particulates to dislodge into the solution.
10/09/2013 03:09 PM EDT
B@B Trade, Inc., Florida is voluntarily recalling all lots of Slim Fortune, Lidiy, and Slim Expert to the consumer level. The FDA laboratory analysis of these dietary supplements found to contain undeclared Sibutramine.
10/08/2013 03:54 PM EDT
Asia Cash & Carry Inc. of Maspeth, New York is voluntarily recalling PRAN brand Spice Powder TURMERIC, Net Wt. 8.82 oz. (250 gm) jars, because it was found to contain high levels of lead that could cause health problems to consumers, particularly infants, small children, and pregnant women if consumed. Recent analysis of the product found it contained 28 parts per million (ppm).
10/16/2013 09:13 AM EDT
BEST VALUE, INC. of Detroit, MI is voluntarily recalling PRAN TURMERIC POWDER because it was found to contain high levels of lead that could cause health problems to consumers, particularly infants, small children, and pregnant women if consumed. The recall was initiated after it was discovered that product contained high levels of lead (53 ppm) based on sampling by Food and Drug Administration.
10/16/2013 03:51 PM EDT
GE Healthcare has initiated a voluntary field corrective action for the Engström ventilator and Aespire View, Aisys, and Avance anesthesia machines due to a potential safety issue. The affected units were manufactured between the dates of April 23, 2013 and July 22, 2013.