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 2901–2920 of 17,529 recalls

August 10, 2022· Nephron Sc Inc

Recalled Item: Ketorolac Tromethamine Injection

The Issue: cGMP Deviations: deviations leading to potential cross-contamination

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

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

Recalled Item: PF-0.125% Bupivacaine HCl Injection

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

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

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

Recalled Item: Trisodium Citrate 0.5% Solution

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

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2022· Akorn, Inc

Recalled Item: Timolol Maleate Ophthalmic Solution

The Issue: Identification of an unknown impurity at the 12-month

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

Class III — Low RiskOngoing
Refund
August 8, 2022· Midlab Incorporated

Recalled Item: Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride

The Issue: CGMP Deviations: Product manufactured using expired active ingredient,

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2022· Midlab Incorporated

Recalled Item: Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in

The Issue: CGMP Deviations: Product manufactured using expired active ingredient,

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

Class II — Potential Health HazardTerminated
Refund
August 4, 2022· LNK International, Inc.

Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets

The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product

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

Class III — Low RiskTerminated
Refund
August 4, 2022· Akron Pharma, Inc.

Recalled Item: Acetaminophen 500 mg tablet

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 4, 2022· Akron Pharma, Inc.

Recalled Item: Acetaminophen 325 mg tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection

The Issue: Temperature Abuse: Product distributed in refrigerated trucks with

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

Class II — Potential Health HazardTerminated
Refund
August 2, 2022· HERON THERAPEUTICS, INC.

Recalled Item: Zynrelef (bupivacaine and meloxicam)

The Issue: Defective Delivery System: An incorrect 10 mL (12

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

Class III — Low RiskTerminated
Refund
August 2, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion 0.05%

The Issue: Lack of Assurance of Sterility: Complaints received of

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

Class II — Potential Health HazardTerminated
Refund
August 1, 2022· Akorn, Inc

Recalled Item: PrednisoLONE Oral Solution USP

The Issue: Defective Container: Product has incomplete induction seals

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

Class II — Potential Health HazardOngoing
Refund
July 29, 2022· Edgewell Personal Care Brands, LLC

Recalled Item: Banana Boat hair & scalp defense

The Issue: Chemical contamination: presence of benzene

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

Class I — Serious Health HazardTerminated
Refund
July 28, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Rifampin Capsules

The Issue: CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine

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

Class II — Potential Health HazardTerminated
Refund
July 27, 2022· Pine Pharmaceuticals, LLC

Recalled Item: Bupivacaine HCl 0.375% w/v and Lidocaine HCl 2% w/v Solution

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
July 27, 2022· Amneal Pharmaceuticals of New York, LLC

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
July 27, 2022· Amerisource Health Services LLC

Recalled Item: Azacitidine for Injection

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
July 25, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pantoprazole Sodium for Delayed-Release Oral Suspension*40 mg* suspension in...

The Issue: Discoloration

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

Class II — Potential Health HazardTerminated
Refund
July 25, 2022· SterRx, LLC

Recalled Item: fentaNYL Citrate in 0.9% Sodium Chloride

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund