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Recent FDA & US Consumer Product Safety Commission Recalls





 


Currently Showing FDA Recall Notices

Note: Updates automatically every five minutes

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Nestlé Prepared Foods Company Announces Allergy Alert and Voluntary Recall Of LEAN CUISINE® Culinary Collection Chicken with Peanut Sauce Recall Due to Package Mislabeling

Filed: Friday,August 22, 2014, 10:59 am

Nestlé Prepared Foods Company, a business unit of Nestlé USA, is initiating the voluntary recall of a limited quantity of LEAN CUISINE® Culinary Collection Chicken with Peanut Sauce/UPC code 13800 10154 because it may contain undeclared shrimp.

Link: http://www.fda.gov/Safety/Recalls/ucm411170.htm

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CloverSnare™ 4-Loop Vascular Retrieval Snare Recall

Filed: Wednesday,August 20, 2014, 8:36 am

On July 10, 2014, Cook Medical initiated a recall of 696 of its CloverSnare™ 4-Loop Vascular Retrieval Snare devices. The device was recalled because of a potential for the loop to separate from the shaft, resulting in loss of device function, potential for embolization of snare fragments and the potential need for intervention to retrieve the separated snare.

Link: http://www.fda.gov/Safety/Recalls/ucm410687.htm

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nSPIRED Natural Foods, Inc. Voluntarily Recalls Certain Retail Lots Of Arrowhead Mills® Peanut Butters, Maranatha® Almond Butters And Peanut Butters And Specific Private Label Nut Butters Because Of Possible Health Risk

Filed: Tuesday,August 19, 2014, 11:32 am

nSpired Natural Foods, Inc. is voluntarily recalling certain retail lots of Arrowhead Mills® Peanut Butters, MaraNatha® Almond Butters and Peanut Butters and specific private label nut butters (listed below) packaged in glass and plastic jars because they have the potential to be contaminated with Salmonella.

Link: http://www.fda.gov/Safety/Recalls/ucm410533.htm

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Voluntary Recall Notice of McCormick Ground Oregano Due to Possible Salmonella Risk

Filed: Thursday,August 14, 2014, 1:04 pm

McCormick & Company, Incorporated is initiating a voluntary recall of McCormick® Ground Oregano, 0.75 oz bottle, UPC 0-523561-6 with code dates BEST BY AUG 21 16 H and AUG 22 16 H due to possible contamination with Salmonella. This recall does not impact any other McCormick Ground, Whole or Oregano Leaves products.

Link: http://www.fda.gov/Safety/Recalls/ucm410107.htm

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Amgen Issues Voluntary Recall of Aranesp® (darbepoetin alfa) (500 mcg) Prefilled Syringes in Several Countries Outside of the United States Due to the Presence of Visible Particulates

Filed: Thursday,August 14, 2014, 6:59 am

Amgen (NASDAQ:AMGN) initiated a voluntary recall on June 26, 2014 for nine packaged lots of Aranesp® (darbepoetin alfa) (500 mcg) prefilled syringes from non-U.S. distributors, wholesalers and a number of hospital pharmacies due to the potential presence of cellulose and/or polyester particles observed in a small number of syringes during a routine quality examination. Lots 1042847, 1044141A, 1044141C, 1044141D, 1046891A, 1046891B, 1047394A, 1047622A, and 1047996A are being recalled as a precautionary measure.

Link: http://www.fda.gov/Safety/Recalls/ucm410011.htm

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Baxter Voluntarily Initiates U.S. Recall of Two Lots of Peritoneal Dialysis Solution Due to Presence of Particulate Matter

Filed: Thursday,August 14, 2014, 6:54 am

Baxter International Inc. announced today it is voluntarily initiating a recall in the United States of two lots of DIANEAL Low Calcium (2.5mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose 5000mL (Ambu-Flex II) to the hospital/user level. The recall is being initiated due to the presence of oxidized stainless steel, garment fiber, and PVC particulate matter identified during the manufacturing process.

Link: http://www.fda.gov/Safety/Recalls/ucm410010.htm

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Baxter Initiates Voluntary Recall of One Lot of 0.9% Sodium Chloride Injection, USP Intravenous (IV) Solution

Filed: Wednesday,August 13, 2014, 10:37 am

Baxter International Inc. announced today it is voluntarily recalling one lot of 0.9% Sodium Chloride Injection, USP 1000 mL, a portion of which was released to customers. The recall is being initiated as a result of particulate matter found near the administration port.

Link: http://www.fda.gov/Safety/Recalls/ucm409899.htm

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Sunfood Recalls Organic Carob Powder Because Of Possible Health Risk

Filed: Tuesday,August 12, 2014, 5:16 pm

Sunfood of El Cajon, CA is recalling Organic Carob Powder, because it has 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.

Link: http://www.fda.gov/Safety/Recalls/ucm409694.htm

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Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Nine Lots of CUBICIN (daptomycin for injection) 500 mg in 10 mL single use vials Following Complaints of Foreign Particulate Matter in Reconstituted Vials

Filed: Saturday,August 9, 2014, 5:51 am

Cubist Pharmaceuticals, Inc. (NASDAQ: CBST) today announced it is voluntarily recalling nine lots of CUBICIN (daptomycin for injection) to the user level following complaints of foreign particulate matter in reconstituted vials. The administration of particulate matter, if present in an intravenous drug, poses a potential safety risk to patients such as a thromboembolism or a life-threatening pulmonary embolism.

Link: http://www.fda.gov/Safety/Recalls/ucm408928.htm

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Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegenESlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk

Filed: Thursday,August 7, 2014, 4:55 pm

Regeneca Worldwide a division of VivaCeuticals, Inc. Las Vegas, NV is conducting a voluntary nationwide recall of its RegenESlim appetite control dietary supplement from lot # EX0616R15814 and lot #11414RE5516 because FDA analysis confirmed the presence of DMAA. DMAA is also known as 1,3-dimethylamylamine, methylhexanamine, or geranium extract. DMAA is commonly used as a stimulant, pre-workout, and weight loss ingredient in dietary supplement products. The Food and Drug Administration (FDA) has warned that DMAA is potentially dangerous to health as it can narrow blood vessels and arteries, which can cause a rise in blood pressure or other cardiovascular problems such as shortness of breath, arrhythmias, tightening in the chest, and heart attack.

Link: http://www.fda.gov/Safety/Recalls/ucm408674.htm

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Cubist Pharmaceuticals Issues Voluntary U.S. Recall Of Certain Lots Of CUBICIN (Daptomycin For Injection) 500 mg In 10 mL Single Use Vials Due To Presence Of Particulate Matter

Filed: Thursday,August 7, 2014, 11:29 am

Cubist Pharmaceuticals, Inc. (NASDAQ: CBST) today announced it is voluntarily recalling certain lots of CUBICIN® (daptomycin for injection) to the user level due to the potential presence of glass particulate matter in vials produced by a contract manufacturer. Please click here for the list of affected CUBICIN lot information.

Link: http://www.fda.gov/Safety/Recalls/ucm408576.htm

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Seoul Shik Poom Inc. Issues Allergy Alert on Undeclared Eggs in Choripdong Chocolate Almond Richmond Ice Bar

Filed: Tuesday,August 5, 2014, 7:14 am

Seoul Shik Poom Inc. of Englewood, NJ is recalling Choripdong Chocolate Almond Richmond Ice Bar (4bags/432ml) because they may contain undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product.

Link: http://www.fda.gov/Safety/Recalls/ucm408027.htm

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Oasis Brands, Inc Recalls Quesito Casero 12oz Because Of Possible Health Risk

Filed: Monday,August 4, 2014, 12:35 pm

Oasis Brands, Inc of Miami, FL is recalling Quesito Casero 12oz with expiration date 09/27/14, because it has the potential to 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.

Link: http://www.fda.gov/Safety/Recalls/ucm407927.htm

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Ortho Molecular Products Issues Allergy Alert On Undeclared Milk In Lifecore Chocolate And Lifecore Complete Chocolate

Filed: Monday,August 4, 2014, 8:51 am

Ortho Molecular Products of Stevens Point, Wisconsin is recalling all lots of LifeCore Chocolate and LifeCore Complete Chocolate because the flavoring may contain undeclared milk. According to food safety standards, people who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

Link: http://www.fda.gov/Safety/Recalls/ucm407872.htm

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New England Greens, LLC dba Vibrant Health Recalls Green Vibrance and Rainbow Vibrance Because of Possible Health Risk

Filed: Friday,August 1, 2014, 6:16 pm

New England Greens of Canaan, Connecticut is recalling 10 lots of Green Vibrance and one lot of Rainbow Vibrance after a former raw material supplier, Raw Deal of Allamuchy, NJ, recalled the Organic Parsley Leaf Powder used to manufacture Green Vibrance and Rainbow Vibrance because of the potential for contamination with Salmonella. Although the possibility is slight that any amount of Salmonella is present in any of the recalled lots of the above-mentioned products, New England Greens is issuing the recall with an abundance of caution for the safety of its consumers.

Link: http://www.fda.gov/Safety/Recalls/ucm407801.htm

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Sunburst Superfoods Recalls Organic Raw Carob Powder Because of Possible Health Risk

Filed: Friday,August 1, 2014, 2:28 pm

Sunburst Superfoods of Tuckahoe, NY, is recalling Sunburst SUPERFOODS Organic Raw Carob Powder sold from March 12, 2014 through July 28th, 2014, because it has 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.

Link: http://www.fda.gov/Safety/Recalls/ucm407794.htm

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Wawona Packing Co. Expands Its Voluntary Recall of Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk

Filed: Friday,August 1, 2014, 8:59 am

Out of an abundance of caution, Wawona Packing Company of Cutler, California is expanding its voluntary recall from July 19, 2014, of whole white and yellow peaches, white and yellow nectarines, plums and pluots due to the potential of the products being contaminated with Listeria monocytogenes.

Link: http://www.fda.gov/Safety/Recalls/ucm407600.htm

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CDPH Warns Consumers Not to Eat VR Green Farms Jarred Food Products Because of Botulism Risk

Filed: Thursday,July 31, 2014, 1:54 pm

California Department of Public Health (CDPH) Director and State Health Officer Dr. Ron Chapman warned consumers today not to eat VR Green Farms jarred food products because they may have been improperly produced, making them susceptible to contamination with Clostridium botulinum.

Link: http://www.fda.gov/Safety/Recalls/ucm407542.htm

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Natural Grocers by Vitamin Cottage Issues Voluntary Recall For Various Chunks of Energy Products Because They Contain Organic Carob Powder From Ciranda, Inc., Which May Be Contaminated With Salmonella

Filed: Thursday,July 31, 2014, 6:34 am

Lakewood, CO. Natural Grocers is issuing a voluntary recall of Chunks of Energy Carob Greens and Chunks of Energy Date / Flax/Tumeric because they contain organic carob powder from Ciranda, Inc., Hudson, WI 54016, which may be contaminated with Salmonella.

Link: http://www.fda.gov/Safety/Recalls/ucm407197.htm

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SW Wisc Dairy Goat Products Coop issues voluntary recall of Raw Goat Milk Mild Cheddar Cheese Lot Code 103-114 because of possible health risk

Filed: Wednesday,July 30, 2014, 1:29 pm

SW Wisc Dairy Goat Products Coop of Mt Sterling, Wisc is recalling Raw Milk Mild Cheddar Cheese Lot Code 103-114 because it may be contaminated with Shiga toxin producing Escherichia coli (STEC) O111:H8 bacteria. This is one of the 6 STEC strains that have been deemed to be of serious health concern as it can cause diarrheal illness, often with bloody stools, and may lead to more severe complications like Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children, the elderly and immunocompromised individuals and can lead to severe kidney damage and even death.

Link: http://www.fda.gov/Safety/Recalls/ucm407355.htm

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Sources: FDA.gov

Sources: CPSC.gov


Note: Data.gov and the Federal Government cannot vouch for the data or analyses derived from these data after the data have been retrieved from Data.gov.





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