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
0 this month

Showing 9321–9340 of 17,529 recalls

March 5, 2018· Novel Laboratories, Inc.

Recalled Item: Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 2, 2018· Renaissance Lakewood, LLC

Recalled Item: Flucanazole Injection

The Issue: Superpotent and Failed Stability Specifications; out of specification

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

Class III — Low RiskTerminated
Refund
February 28, 2018· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets

The Issue: Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL

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

Class III — Low RiskTerminated
Refund
February 26, 2018· Mckesson Packaging Services

Recalled Item: RANITIDINE Tablets

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardTerminated
Refund
February 26, 2018· Paddock Laboratories, LLC.

Recalled Item: Evamist (estradiol transdermal spray)

The Issue: Defective Delivery System: Potential that cracks in the

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

Class II — Potential Health HazardTerminated
Refund
February 23, 2018· AstraZeneca Pharmaceuticals LP

Recalled Item: Lynparza (olaparib) capsules 50 mg

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
February 23, 2018· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Coppertone Kids Sunscreen Spray (avobenzone 3%

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardTerminated
Refund
February 22, 2018· SCA Pharmaceuticals, LLC.

Recalled Item: labetalol HCl injection 20 mg/4 mL (5mg/mL)

The Issue: Labeling; Incorrect or Missing Lot number/Expiration Date; some

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

Class III — Low RiskTerminated
Refund
February 21, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection

The Issue: Labeling: Label mix-up - A complaint was received

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

Class II — Potential Health HazardTerminated
Refund
February 21, 2018· Akorn, Inc.

Recalled Item: Atropine Sulfate Ophthalmic 1% Solution

The Issue: Failed Stability Specification: OOS low viscosity results discovered

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

Class III — Low RiskTerminated
Refund
February 20, 2018· Hospira Inc. A Pfizer Company

Recalled Item: Labetalol Hydrochloride Injection

The Issue: Defective Container: Cracked glass at the rim surface

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

Class II — Potential Health HazardTerminated
Refund
February 19, 2018· Kalchem International, Inc.

Recalled Item: Vardenafil HCl

The Issue: cGMP Deviations: Lack of stability data and controls

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

Class II — Potential Health HazardTerminated
Refund
February 16, 2018· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Irrigation USP

The Issue: Presence of Particulate Matter: Customer complaint of particulate

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

Class II — Potential Health HazardTerminated
Refund
February 15, 2018· Apollo Care

Recalled Item: Vancomycin 1g added to 250mL of 0.9% Sodium Chloride IV bag

The Issue: Stability Data Does Not Support Expiry: 90-day beyond

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

Class II — Potential Health HazardTerminated
Refund
February 15, 2018· Apollo Care

Recalled Item: Vancomycin 1.25g added to 250mL of 0.9% Sodium Chloride IV bag

The Issue: Stability Data Does Not Support Expiry: 90-day beyond

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

Class II — Potential Health HazardTerminated
Refund
February 15, 2018· Medline Industries Inc

Recalled Item: PVP Scrub Solution

The Issue: Subpotent Drug: product not meeting the iodine assay

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

Class II — Potential Health HazardTerminated
Refund
February 14, 2018· Bella All Natural

Recalled Item: Bella Capsules

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund