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 2381–2400 of 17,529 recalls

February 23, 2023· Nutraceutical Corporation

Recalled Item: NatraBio

The Issue: CGMP Deviations: Raw material recalled by repackager, due

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

Class II — Potential Health HazardOngoing
Refund
February 23, 2023· Nutraceutical Corporation

Recalled Item: NaturalCare

The Issue: CGMP Deviations: Raw material recalled by repackager, due

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

Class II — Potential Health HazardOngoing
Refund
February 23, 2023· The Harvard Drug Group

Recalled Item: Carbidopa and Levodopa Tablets

The Issue: Packaging defect: observed packaging defect, blister packaging inadequately

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

Class II — Potential Health HazardTerminated
Refund
February 22, 2023· Teva Pharmaceuticals USA Inc

Recalled Item: Metformin hydrochloride Extended-Release Tablets

The Issue: CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in

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

Class II — Potential Health HazardTerminated
Refund
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 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
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl in 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
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Diltiazem HCl in 0.7% 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
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 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
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 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
February 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 21, 2023· Padagis US LLC

Recalled Item: Evamist (estradiol transdermal spray)

The Issue: Failed Content Uniformity Specifications: The Spray Content Uniformity

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

Class III — Low RiskOngoing
Refund
February 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardTerminated
Refund
February 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 0.5 mg per 5 mL (100 mcg/mL)

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardTerminated
Refund
February 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardTerminated
Refund
February 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardTerminated
Refund
February 17, 2023· Akron Pharma, Inc.

Recalled Item: DIBUCAINE 1% HEMORRHOIDAL OINTMENT

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 RiskTerminated
Refund
February 17, 2023· Sciegen Pharmaceuticals Inc

Recalled Item: Gabapentin Tablets

The Issue: Presence of Foreign Tablets/Capsules: Pharmacist reported presence of

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

Class III — Low RiskTerminated
Refund
February 15, 2023· Azurity Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection

The Issue: cGMP: complaints of crystals not redissolving into solution

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

Class II — Potential Health HazardTerminated
Refund