RSSDrug Recalls

Stemvida International Corporation Recalls Stemalive 90 Capsules

Stemvida International Corporation Recalls Stemalive 90 Capsules

| January 18, 2014 | 0 Comments

Stemvida International Corporation of Ontario California is recalling StemAlive 90 Capsules, because it contains undeclared milk. People who have an allergy or severe sensitivity to milk (bovine colostrum) run the risk of serious or life-threatening allergic reaction if they consume this product. The product is in a white plastic bottle with white lid, the brand […]

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Midwest Wholesale Issues Voluntary Recall of Various Products

Midwest Wholesale Issues Voluntary Recall of Various Products

| January 13, 2014 | 0 Comments

Midwest Wholesale is voluntarily recalling the following products and Lot numbers. List of Products included in this Recall: Boost Ultra 12 pill bottle, Lot#B70130, Exp 03/15 3 pill bottle, Lot#B70130, Exp 3/2015 1 pill pack, Lot#06012011, Exp 6/2014 XZone Gold 1 pill pack, Lot#130710GL, Exp 7/31/18 Sexy Monkey 1 pill pack, Exp 12/31/14 Triple MiracleZen […]

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Baxter Recalls Select Lots of Premix Parenteral Nutrition

Baxter Recalls Select Lots of Premix Parenteral Nutrition

| January 3, 2014 | 0 Comments

Baxter International Inc. ahs announced it has initiated a voluntary recall in the United States of two lots of CLINIMIX and one lot of CLINIMIX E Injection premix parenteral nutrition products to the user level due to complaints of particulate matter found in the products. If infused, particulate matter may result in blockages of blood […]

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Deseo Rebajar Inc. Issues Voluntary Recall of Burn 7 Capsules

Deseo Rebajar Inc. Issues Voluntary Recall of Burn 7 Capsules

| December 24, 2013 | 0 Comments

Deseo Rebajar Inc., is voluntarily recalling lot #MFD: 07.18.2013 (Exp: 07.17.2015) of Burn 7 Capsules to the consumer level. The FDA laboratory analysis of this dietary supplement found the Burn 7 Capsules product to contain undeclared Sibutramine. Sibutramine was a previously approved controlled substance for the treatment of obesity that was removed from the U.S. […]

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Consumers Warned to Immediately Stop Using Mass Destruction

Consumers Warned to Immediately Stop Using Mass Destruction

| December 24, 2013 | 0 Comments

The U.S. Food and Drug Administration is advising consumers to immediately stop using a product called Mass Destruction, marketed as a dietary supplement for muscle growth. The product is labeled to contain at least one synthetic anabolic steroid and has been linked to at least one reported serious illness. The FDA was alerted by the […]

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Hospira Recalls One Lot of Lidocaine Hcl Injection, Usp, 2%, 5 Ml in 5 Ml Vial

Hospira Recalls One Lot of Lidocaine Hcl Injection, Usp, 2%, 5 Ml in 5 Ml Vial

| December 23, 2013 | 0 Comments

Hospira, Inc. has announced it will initiate a voluntary nationwide recall to the user level for one lot of Lidocaine HCl Injection, USP, 2%, 5 mL Single-Dose Vial (NDC 0409-2066-05), Lot 32-135-DD, expiration date 1AUG2015. The recall is due to a reddish orange particulate on the inner surface and floating in the solution. If particulate […]

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Abrams Royal Pharmacy Recalls All Lots of Unexpired Sterile Products

Abrams Royal Pharmacy Recalls All Lots of Unexpired Sterile Products

| December 19, 2013 | 0 Comments

Abrams Royal Pharmacy is voluntarily recalling all unexpired lots of sterile products dispensed nationwide due to concerns of lack of sterility assurance. All unexpired lots of sterile compounded products are subject to the recall. Sterile products are injectable medications, IVs, eye drops, pellet implants, nasal sprays, inhalation solutions, and eye ointments. All recalled products have […]

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