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
1 this month

Showing 7741–7760 of 17,529 recalls

February 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 10 Units added to NS 1000 mL (oxytocin and

The Issue: Superpotent Drug: product may contain concentrations of oxytocin

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

Class III — Low RiskTerminated
Refund
February 6, 2019· Advanced Pharma Inc.

Recalled Item: Fentanyl in 0.9% Sodium Chloride QS 0.5 mL

The Issue: Labeling: Incorrect expiration date

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

Class II — Potential Health HazardTerminated
Refund
February 6, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules USP

The Issue: Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain

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

Class III — Low RiskTerminated
Refund
February 4, 2019· Akorn Inc

Recalled Item: Moisturizing Lubricant Eye Drops

The Issue: Failed Stability Specification: out of specification results for

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2019· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
February 1, 2019· Mylan Institutional Inc

Recalled Item: Levoleucovorin Injection

The Issue: Presence of Particulate Matter: particulate matter identified as

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

Class I — Serious Health HazardTerminated
Refund
February 1, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Moxifloxacin Ophthalmic Solution USP

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
February 1, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray

The Issue: Defective Container: Potential for broken glass in the

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

Class II — Potential Health HazardTerminated
Refund
January 31, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Diltiazem HCl CD capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 29, 2019· US Compounding Inc

Recalled Item: Ephedrine Sulfate

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
January 28, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Bimatoprost Ophthalmic Solution 0.03%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 25, 2019· Akorn Inc

Recalled Item: Clobetasol Propionate Emollient Cream 0.05%

The Issue: Failed Stability Specification; out of specification (OOS) results

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

Class III — Low RiskTerminated
Refund
January 25, 2019· Natures Rx

Recalled Item: the silver bullet 10x Capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
January 24, 2019· US Compounding Inc

Recalled Item: LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%)

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
January 24, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: BromSite (bromfenac ophthalmic solution) 0.075%

The Issue: Bromfenac Ophthalmic Solution, 0.075% (Sterile 5 mL) may

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

Class II — Potential Health HazardTerminated
Refund