Marlex Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Digoxin Tablets USP, 0.125mg and Digoxin Tablets USP, 0.25mg Due to Label Mix-Up

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New Castle, Delaware, Marlex Pharmaceuticals, Inc. is voluntarily recalling one lot of Digoxin Tablets USP, 0.125mg and one lot of Digoxin Tablets USP, 0.25mg to the consumer level due to Label Mix-Up. Bottles of Digoxin Tablets, USP 0.125mg s are incorrectly labeled and contain Digoxin Tablets USP,

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

Universal Meditech Inc. Issues Nationwide Recall of All Products Manufactured Between March 2021 and November 2022

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On July 1, 2023, Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: i.The company is going out of business, hence would not be able to continue fulfilling any post-market responsibilities of

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

Dr. Berne’s Whole Health Products Issues Voluntary Nationwide Recall of Dr. Berne’s MSM Drops 5% and 15% Solution Eye Drops Due to Bacterial and Fungal Contamination

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Tesuque, NM, Dr. Berne’s Whole Health Products is voluntarily recalling all lots of MSM DROPS 5%,15% Solution, Dr. Berne’s Organic Castor Oil Eye Drops and Dr. Berne’s MSM MIST 15% Solution to the consumer level.

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

Furst-McNess Company Recalls Goat Starter Because of Possible Monovet® 90 (Monensin) Health Risk

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Monensin is an FDA-approved drug for use in certain animal feeds. However, if the feed contains excessive amounts of the drug, the feed can cause monensin toxicity in a number of animal species including goats. Goats ingesting excessive levels of monensin in feed are susceptible to injury and death.

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

Hua Da Trading Inc dba Wefun Inc Issues Voluntary Nationwide Recall of WEFUN Capsules Due to Presence of Undeclared Sildenafil

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Brooklyn, New York, WEFUN Inc is voluntarily recalling 300 Boxes of WEFUN Capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) inhibitor found in FDA-approved products for the trea

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

WEFUN Inc Issues Voluntary Nationwide Recall of WEFUN Capsules Due to Presence of Undeclared Sildenafil

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Brooklyn, New York, WEFUN Inc is voluntarily recalling 300 Boxes of WEFUN Capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) inhibitor found in FDA-approved products for the trea

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

Texas Tamale Co. Issues Allergy Alert on Undeclared Milk in Texas Tamale Black Bean Tamales

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Texas Tamale Co. located in Houston, Texas, is instituting a recall for one lot of Texas Tamale Black Bean Tamales due to the potential presence of an undeclared milk allergen. Hatch Green Chile and Cheese Tamales were mistakenly packaged in Black Bean Tamale Bags. Individuals with an allergy or hei

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

Inmar Supply Chain Solutions, LLC, Issues a Voluntary Recall of Product Stored at its Arlington, Texas Facility Due to Conditions at the Facility

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Inmar Supply Chain Solutions, LLC (“Inmar”), is voluntarily recalling FDA regulated products* contained in pallets stored in Inmar’s Arlington, Texas facility between May 1, 2022, and June 30, 2023, the (“FDA Recalled Products”). The FDA Recalled Products were stored in this facility during a time

Source: FDA Food Safety Recalls RSS Feed

Twin City Foods, Inc., Recalls Frozen Super Sweet Corn and Mixed Vegetables Because of Possible Health Risk

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Twin City Foods, Inc. of Stanwood, Washington, is voluntarily recalling a limited quantity of Not-Ready-To Eat Individually Quick Frozen (IQF) Super Sweet Cut Corn and Mixed Vegetables in retail bags, due to a potential for these products to be contaminated with Listeria monocytogenes. Listeria mono

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

Stonewall Kitchen Issues Allergy Alert on Undeclared Soy, Wheat, and Peanuts in Peanut Butter Maltballs (6oz.)

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Stonewall Kitchen of York, Maine is recalling a limited amount of their Peanut Butter Maltballs (6oz.) because the product contains undeclared allergens: Soy, Wheat, Peanuts. People who have an allergy or severe sensitivity to peanuts, wheat, and/or soy run the risk of serious or life-threatening al

Source: FDA Food Safety Recalls RSS Feed