Drug Recalls

Here you'll find every drug recall the FDA has issued, including prescription medications, over-the-counter drugs, compounded pharmacy products, and dietary supplements. We've been tracking these since 2006 and our database updates several times a day so you're always looking at current information.

Drugs get recalled for a number of reasons: contamination during manufacturing, incorrect potency or dosage, failed quality testing (like dissolution or stability tests), sterility problems in injectable products, or labeling and packaging errors that could cause someone to take the wrong dose. If you find a product on this list that you use, please follow the instructions provided by the FDA to take the necessary precautions.

17,529 total recalls
0 this month

Showing 12321–12340 of 17,529 recalls

August 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Burn Fat Now Dietary Supplement packaged in

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Fataway Ultimate Stack with Chromium

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Allergan Sales, LLC

Recalled Item: BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic ointment

The Issue: Presence of Particulate Matter: Due to customer complaints

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Naturally The Natural Alternative AM Dietary Supplement

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim MaxOut Body Max Out FX Fat Burner

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Allergan Sales, LLC

Recalled Item: Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant

The Issue: Presence of Particulate Matter: Due to customer complaints

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Xcellerator (product not labeled)

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: The Store Thin and Slim Thermogenic Fat Burner Dietary Supplement

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Methyldrene Original 25 Ephedra ECA Stack Extra-Potent Fat Burner Dietary

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: MetaPro 360 Metabolic Accelerator Dietary Supplement packaged in 120 capsule

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: The People's Chemist Thermo FX Barely Legal Thermogenic Aid

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Extreme Stack Fat Burner Dietary Supplement packaged

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 21, 2015· Akorn, Inc.

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution

The Issue: Defective Container: Product missing safety seal around the

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskTerminated
Refund
August 21, 2015· Cantrell Drug Company

Recalled Item: Atropine Sulfate Injection Solution

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 21, 2015· Silarx Pharmaceutical, Inc.

Recalled Item: Lamivudine Oral Solution

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskTerminated
Refund
August 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL citrate in 0.9% Sodium Chloride Injection

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
August 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution

The Issue: Lack of Assurance of Sterility; potential exposure to

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
August 21, 2015· Cantrell Drug Company

Recalled Item: MIDAZolam HCl 0.1 mg/mL in 5% DEXTROSE 2.5 mL syringe

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
August 21, 2015· Cantrell Drug Company

Recalled Item: LIDocaine HCl 1% BUFFERED WITH SODIUM BICARBONATE Injection

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund