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 9621–9640 of 17,529 recalls

November 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: 7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule

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

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

Class II — Potential Health HazardTerminated
Refund
November 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Anastrozole SR 1 mg Capsules

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

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

Class II — Potential Health HazardTerminated
Refund
November 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Hydroxocobalamin 1 mg/mL 30 mL Vial For IM Use

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

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

Class II — Potential Health HazardTerminated
Refund
November 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Acetate 3 mg/ GHRP6 3 mg

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

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

Class II — Potential Health HazardTerminated
Refund
November 13, 2017· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
November 13, 2017· Elite Laboratories Inc.

Recalled Item: Isradapine Capsules USP 2.5 mg

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 11, 2017· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection

The Issue: Superpotent

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

Class III — Low RiskTerminated
Refund
November 10, 2017· Baxter Healthcare Corporation

Recalled Item: Nexterone (amiodarone HCl) Premixed Injection

The Issue: Presence of Particulate Matter:Particulate identified as polyethylene, the

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

Class I — Serious Health HazardTerminated
Refund
November 10, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Bayer Chewable Low Dose Aspirin 81 mg Orange Flavored 36 tablets

The Issue: Failed Stability Specifications

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

Class III — Low RiskTerminated
Refund
November 9, 2017· Kareway Products Inc

Recalled Item: GERICARE Eyewash

The Issue: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans

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

Class I — Serious Health HazardTerminated
Refund
November 9, 2017· Teva Pharmaceuticals USA

Recalled Item: Clozapine Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
November 9, 2017· Mayne Pharma Inc

Recalled Item: Liothyronine Sodium Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2017· L. Perrigo Company

Recalled Item: Maximum Strength Zephrex-D

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardTerminated
Refund
November 6, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection

The Issue: Superpotent

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

Class III — Low RiskTerminated
Refund
November 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 3, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: bupPROPion HCL Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 3, 2017· Ridge Properties, LLC

Recalled Item: Extra Strength Naturally HL Liquid Hemorrhoid Relief Gel

The Issue: GMP Deviations: inadequate manufacturing control processes

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

Class II — Potential Health HazardTerminated
Refund
November 3, 2017· Ridge Properties, LLC

Recalled Item: Extra Strength Naturally HL Bed Sore Relief Cream with Added Lidocaine

The Issue: GMP Deviations: inadequate manufacturing control processes

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

Class II — Potential Health HazardTerminated
Refund
November 3, 2017· Ridge Properties, LLC

Recalled Item: Extra Strength Naturally HL Hemorrhoid Numbing with Lidocaine

The Issue: GMP Deviations: inadequate manufacturing control processes

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

Class II — Potential Health HazardTerminated
Refund