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
2 this month

Showing 2741–2760 of 17,529 recalls

November 28, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection

The Issue: Defective Container: Complaints received of vial breakage and

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

Class I — Serious Health HazardTerminated
Refund
November 25, 2022· B. Braun Medical, Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx

The Issue: Lack of sterility assurance: Bags have the potential

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

Class II — Potential Health HazardTerminated
Refund
November 23, 2022· Heritage Pharmaceuticals Inc

Recalled Item: Desmopressin Acetate Tablets 0.2mg

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
November 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection

The Issue: Subpotent Drug: Testing results below the defined limit

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

Class II — Potential Health HazardTerminated
Refund
November 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection

The Issue: Subpotent Drug: Testing results below the defined limit

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

Class II — Potential Health HazardTerminated
Refund
November 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection

The Issue: Subpotent Drug: Testing results below the defined limit

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

Class II — Potential Health HazardTerminated
Refund
November 22, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Leakage of 0.9%

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

Class II — Potential Health HazardOngoing
Refund
November 21, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 16, 2022· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system)

The Issue: Defective Delivery System: Recalled lot was found to

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

Class II — Potential Health HazardOngoing
Refund
November 14, 2022· Acella Pharmaceuticals, LLC

Recalled Item: Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads

The Issue: Subpotent drug: Out of specification for assay at

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

Class III — Low RiskTerminated
Refund
November 14, 2022· Acella Pharmaceuticals, LLC

Recalled Item: Phenytoin Sodium Injection

The Issue: Labeling: Not elsewhere classified; the product is being

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

Class III — Low RiskTerminated
Refund
November 14, 2022· Acella Pharmaceuticals, LLC

Recalled Item: Phenytoin Sodium Injection

The Issue: Labeling: Not elsewhere classified; the product is being

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

Class III — Low RiskTerminated
Refund
November 10, 2022· Par Formulations Private Limited

Recalled Item: Phenoxybenzamine Hydrochloride Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
November 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Neostigmine Methylsulfate Injection

The Issue: CGMP Deviations: Potential for cross contamination due to

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

Class II — Potential Health HazardTerminated
Refund
November 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Labetalol HCl Injection

The Issue: CGMP Deviations: Potential for cross contamination due to

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

Class II — Potential Health HazardTerminated
Refund
November 9, 2022· DISCOVERY PHARMA LLC

Recalled Item: Conzerol zero molluscum contagiosum

The Issue: CGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
November 9, 2022· Lannett Company Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Capsules

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskTerminated
Refund
November 9, 2022· Lannett Company Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Capsules

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskTerminated
Refund
November 9, 2022· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost (0.5/0.005%) ophthalmic drops

The Issue: Subpotent Drug: The batches contain less than 90%

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

Class II — Potential Health HazardTerminated
Refund
November 9, 2022· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of assurance of sterility: Bags have the

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

Class II — Potential Health HazardOngoing
Refund