Kula Brands LLC Issues Allergy Alert on Undeclared Coconut and Milk in Kula Can Pina Colada + Kratom Seltzer

/in , /by
Kula Brands LLC is recalling Kula Can - Pina Colada + Kratom Seltzer due to the presence of undeclared tree nuts (coconut) and milk. People who have an allergy or severe sensitivity to tree nuts (coconut) and/or milk, run the risk of serious or life-threatening allergic reaction if they consume this

Source: FDA Food Safety Recalls RSS Feed

Voluntary Recall of Certain Over-the-Counter Drugs and Medical Devices

/in /by
Family Dollar is initiating a voluntary retail-level product recall of certain over-the-counter drugs and medical devices regulated by the U.S. Food and Drug Administration (FDA). These items were stored outside of labeled temperature requirements by Family Dollar and inadvertently shipped to certai

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

Orgain Issues Allergy Alert on Undeclared Sesame in Organic Plant Protein + Superfoods Powder, Creamy Chocolate Fudge Sold in Costco Warehouse Stores

/in /by
Orgain LLC of Irvine, CA is voluntarily recalling a limited production run of its Organic Protein Powder + Superfoods, Creamy Chocolate Fudge flavor, because it may contain an undeclared sesame allergen

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

Cookies-N-Milk Issues Allergy Alert on Undeclared Peanuts in Chocolate Chip Edible Cookie Dough

/in /by
Cookies-N-Milk, of McKinney, TX is recalling their 6oz cups of "Chocolate Chip Edible Cookie Dough" because it may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.

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

Hospira, Inc. Issues a Voluntary Nationwide Recall for 4.2% Sodium Bicarbonate Injection, USP and 1% and 2% Lidocaine HCl Injection, USP Due to the Potential for Presence of Glass Particulate Matter

/in /by
Hospira, Inc., a Pfizer company, is voluntarily recalling the lots listed in the table below of 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP,
50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level. The recall was initiated d

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

Biomic Sciences Issues Voluntary Nationwide Recall of ION* Sinus Support, ION* Sinus, and Restore Sinus Spray Products Due to Microbial Contamination

/in /by
Charlottesville, VA - Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION* Sinus, and Restore Sinus Spray products to the consumer level. FDA testing found the product to contain microbial contamination identified as Microbacterium sp., Fictibacillus sp., Bacillus sp.,

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

Merck Animal Health Expands Voluntary Recall with Four Additional Lots of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) in the U.S., Due to Presence of Particulate Matter

/in /by
Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA (NYSE:MRK), is voluntarily recalling four additional batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for i

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

Biomic Sciences Issues Voluntary Nationwide Recall of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray Products Due to Microbial Contamination

/in /by
Charlottesville, VA - Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray products to the consumer level. FDA testing found the product to contain microbial contamination identified as Microbacterium sp., Fictibacillus sp., Bacillus sp.,

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

KVK-Tech, Inc. Issues Voluntary Nationwide Recall of One Lot of Betaxolol Tablets, USP 10 mg (Batch Number: 17853A) as a Precautionary Measure Due to a Single Foreign Tablet Found During the Line Clearance After the Batch was Packaged

/in /by
Newtown, Pennsylvania, KVK-Tech, Inc. is voluntarily recalling one lot (Batch Number: 17853A; “the batch”) of Betaxolol Tablets, USP 10 mg, White, Round, film coated biconvex tablets, debossed “K” above bisect “13” on one side and plain on the other side” to the consumer level. The batch was distrib

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

Medtronic Notification of Stolen Defective Products – Potentially Defective McGRATH™ MAC Video Laryngoscopes

/in /by
Medtronic is issuing this notification to inform the public of stolen defective McGRATH™ MAC video laryngoscopes that have been offered for sale illegally by unauthorized third parties through various social media platforms. These affected products did not pass Medtronic’s rigorous quality tests est

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