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 541–560 of 17,529 recalls

June 24, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg

The Issue: Product Mix Up: This product is being recalled

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
June 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules

The Issue: Defective container; blister packaging inadequately sealed

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

Class II — Potential Health HazardOngoing
Refund
June 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules

The Issue: Defective container; blister packaging inadequately sealed

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

Class II — Potential Health HazardOngoing
Refund
June 16, 2025· Qualgen, LLC

Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials

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 RiskOngoing
Refund
June 16, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
June 16, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP

The Issue: Lack of assurance of sterility: pinholes, within the

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

Class II — Potential Health HazardOngoing
Refund
June 11, 2025· Macleods Pharmaceuticals Ltd

Recalled Item: Famciclovir Tablets

The Issue: Presence of Foreign Substance- Black hair strand found

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

Class III — Low RiskOngoing
Refund
June 11, 2025· Orient Pharma Co., Ltd. Yunlin Plant

Recalled Item: Pitavastatin Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskOngoing
Refund
June 11, 2025· Orient Pharma Co., Ltd. Yunlin Plant

Recalled Item: Pitavastatin Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskOngoing
Refund
June 10, 2025· IMMUNOCORE, LLC

Recalled Item: KIMMTRAK (tebentafusp-tebn) Injection

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
June 6, 2025· Church & Dwight Inc

Recalled Item: Orajel Baby

The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of

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

Class I — Serious Health HazardOngoing
Refund
June 6, 2025· Church & Dwight Inc

Recalled Item: ZICAM COLD REMEDY MEDICATED NASAL SWABS

The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of

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

Class I — Serious Health HazardOngoing
Refund