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 17161–17180 of 17,529 recalls

July 12, 2012· Axcentria Pharmaceuticals LLC

Recalled Item: Major brand Infants' Mapap

The Issue: Labeling; labeled with incorrect EXP Date; Incorrect expiration

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

Class III — Low RiskTerminated
Refund
July 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification

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

Class II — Potential Health HazardTerminated
Refund
July 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification

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

Class II — Potential Health HazardTerminated
Refund
July 11, 2012· Actavis

Recalled Item: Fentanyl Transdermal System

The Issue: Subpotent; some patches may not contain fentanyl gel

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.112 mg.

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.137 mg.

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.300 mg.

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.088 mg.

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg.

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.125 mg.

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 9, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: cGMP Deviations; does not meet in process specification

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

Class II — Potential Health HazardTerminated
Refund
July 6, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCORTISONE and ACETIC ACID OTIC SOLUTION

The Issue: Impurities/Degradation Products: Out of specificiation results for impurities

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

Class III — Low RiskTerminated
Refund
July 6, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: HYDROXYZINE HYDROCHLORIDE ORAL SOLUTION

The Issue: Impurities/Degradation Products: High Out of Specification results for

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

Class III — Low RiskTerminated
Refund
July 6, 2012· Glenmark Generics Inc., USA

Recalled Item: NAPROXEN TABLETS USP

The Issue: Labeling: Label Mix-Up: Bottles labeled as Naproxen Tablets

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

Class II — Potential Health HazardTerminated
Refund
July 5, 2012· Ben Venue Laboratories Inc

Recalled Item: Leucovorin Calcium Injection USP

The Issue: Presence of Particulate Matter: visible crystalline particulates and

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

Class II — Potential Health HazardTerminated
Refund