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 12401–12420 of 17,529 recalls

July 29, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP

The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations

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

Class II — Potential Health HazardTerminated
Refund
July 29, 2015· Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Recalled Item: Lisinopril 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 29, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP

The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations

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

Class II — Potential Health HazardTerminated
Refund
July 28, 2015· Novartis Pharmaceuticals Corp.

Recalled Item: Dexmethylphenidate HCl Extended-Release

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Meijer Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Wal-itin Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Health Mart Pharmacy loratadine orally disintegrating tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Fred's Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Safeway Care Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: CareOne Original Prescription Strength

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: QC Quality Choice Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Equaline Original Prescription Strength

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Sunmark loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Leader Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Health Best Choice Care

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Major loratadine orally disintegrating tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Up&Up loratadine orally disintegrating tablets

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund
July 28, 2015· Ohm Laboratories, Inc.

Recalled Item: Rite Aid Pharmacy loratadine orally disintegrating tablets USP

The Issue: Superpotent Drug: Out Of Specification (OOS) result for

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

Class III — Low RiskTerminated
Refund