Pfizer Issues a Voluntary Nationwide Recall for Twelve Lots of CHANTIX® (Varenicline) Tablets Due to N-Nitroso Varenicline Content

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Pfizer is voluntarily recalling two lots of Chantix 0.5mg Tablets, two lots of Chantix 1 mg Tablets, and eight lots of a Chantix kit of 0.5mg/1 mg Tablets to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-varenicline, above the Pfizer established Acceptable Daily I

Source: Food and Drugs Administration--Recalls/Safety Alerts

BrightFarms Announces Voluntary Recall of Packaged Salad Greens Sold in Illinois, Wisconsin, Iowa, Indiana and Michigan

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BrightFarms today initiated a voluntary recall of packaged salad greens produced in its Rochelle, Illinois (Ogle County) greenhouse farm sold in Illinois, Wisconsin, Iowa, Indiana and Michigan because it has the potential to be contaminated with Salmonella.

Source: Food and Drugs Administration--Recalls/Safety Alerts

BrightFarms Announces Voluntary Recall of Packaged Salad Greens Sold in Illinois, Wisconsin, Iowa and Indiana

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BrightFarms today initiated a voluntary recall of packaged salad greens produced in its Rochelle, Illinois (Ogle County) greenhouse farm sold in Illinois, Wisconsin, Iowa and Indiana because it has the potential to be contaminated with Salmonella.

Source: FDA Food Safety Recalls RSS Feed

Johnson & Johnson Consumer Inc. Issues Voluntary Recall of Specific NEUTROGENA® and AVEENO® Aerosol Sunscreen Products Due to the Presence of Benzene

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Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and fol

Source: Food and Drugs Administration--Recalls/Safety Alerts

5000 Years Foods, Inc. Recall Cabbage Kimchi Because of Possible of Health Risk

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5000 YEARS FOODS, INC. of CHICAGO, ILLINOIS is recalling SLICED CABBAGE KIMCHI, WHOLE CABBAGE KIMCHI, JULRADO WHOLE CABBAGE KIMCHI, JULRADO SLICED CABBAGE KIMCHI, NO MSG WHOLE CABBAGE KIMCHI, NO MSG SLICED CABBAGE KIMCHI, NO MSG JULRADO WHOLE CABBAGE KIMCHI, NO MSG JULRADO SLICED CABBAGE KIMCHI, WHI

Source: FDA Food Safety Recalls RSS Feed

Innoveix Pharmaceuticals, Inc. Issues Voluntary Recall of All Sterile Compounded Drug Products Due to A Lack of Sterility Assurance

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Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots of sterile compounded drug products, within expiry. The products are being recalled due to a lack of assurance of sterility. These concerns arose following a routine inspection of the pharmacy by FDA.

Source: Food and Drugs Administration--Recalls/Safety Alerts

LSG Sky Chefs Recalls Circle K Brand Chicken Salad Sandwich Because of Possible Health Risk

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LSG Sky Chefs announced today that it is issuing a voluntary recall of its Chicken Salad Sandwich 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 wit

Source: Food and Drugs Administration--Recalls/Safety Alerts

LSG Sky Chefs Recalls Circle K Brand Chicken Salad Sandwich Because of Possible Health Risk

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LSG Sky Chefs announced today that it is issuing a voluntary recall of its Chicken Salad Sandwich 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 wit

Source: Food and Drugs Administration--Recalls/Safety Alerts

Ardil Comercial Issues Voluntary Nationwide Recall of Limar Hand Sanitizer Packaged in 4 oz Bottles Because They Resemble Drink Containers

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Santo Domingo, Dominican Republic – Ardil Comercial is voluntarily recalling one lot of Limar Hand Sanitizer, packaged in 4 oz bottles to the consumer level. The hand sanitizer is being recalled because it is packaged in containers that resemble water bottles. The product poses a risk of ingestion

Source: Food and Drugs Administration--Recalls/Safety Alerts

Teva Initiates Voluntary Nationwide Recall of One Lot of Topotecan Injection 4 mg/4 mL (1 mg/mL) Due to Presence of Particulate Matter

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Teva Pharmaceuticals has initiated a voluntary recall of lot 31328962B of Topotecan Injection 4 mg/4 mL (1 mg/mL), to the retail/institutional level in the United States. This voluntary recall was initiated based on a complaint received from a pharmacy after a single glass particle was observed ins

Source: Food and Drugs Administration--Recalls/Safety Alerts