Merck Animal Health Issues Voluntary Recall for Three Lots of BANAMINE® / BANAMINE®-S (Flunixin Meglumine Injection) in the U.S., Due to Presence of Particulate Matter

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 three batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for injection i

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

Weis Markets Issues an Allergy Alert for Weis Quality Premium Brownie Moose Tracks Ice Cream Due to Undeclared Egg Allergen

Weis Markets Inc. of Sunbury, PA today said it is recalling containers of Weis Quality Brownie Moose Tracks Ice Cream (48oz) because the product may contain undeclared EGG. People who have an allergy or severe sensitivity to EGG run the risk of serious or life-threatening allergic reactions if they

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

TODORGANIC INC Retira Del Mercado Producto De Nuez De La India Seeds Debido a Posible Riesgo Para La Salud

TODORGANIC INC Middleburg FL está retirando del mercado sus semillas Nuez de la India porque un análisis de la FDA ha determinado que las semillas parecen ser Thevetia peruviana o adelfa amarilla. Se sabe que todas las partes de la planta de adelfa amarilla contienen glucósidos cardíacos que son alt

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

TODORGANIC INC. Recalls Nuez De La India Seeds Product Due to Possible Health Risk

TODORGANIC INC Middleburg FL is recalling its Nuez de la India Seeds because FDA analysis has determined that the seeds appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides that are highly toxic to humans and animals. Ing

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

The Ice Cream House is Voluntarily Recalling All Dairy Ice Cream Products and Non-Dairy [Parve] Frozen Dessert Products Due to Potential Health Risk in Regards to Listeria Monocytogenes

The Ice Cream House is voluntarily recalling all Dairy Ice Cream Products and Non-dairy [Parve] frozen Dessert products due to potential health risk in regards to Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, fra

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

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

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

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

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

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

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