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 10821–10840 of 17,529 recalls

October 13, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Olanzapine tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 13, 2016· Amerisource Health Services

Recalled Item: AHP NIFEdipine Capsules

The Issue: Presence of Foreign Tablets/Capsules

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

Class III — Low RiskTerminated
Refund
October 12, 2016· Pharm D Solutions, LLC

Recalled Item: HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial

The Issue: Labeling; Error on Declared Strength; product description incorrectly

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

Class III — Low RiskTerminated
Refund
October 12, 2016· Pharmedium Services, LLC

Recalled Item: Succinylcholine Chloride

The Issue: Lack of Assurance of Sterility: A portion of

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

Class II — Potential Health HazardTerminated
Refund
October 12, 2016· Pharm D Solutions, LLC

Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame Oil

The Issue: Undeclared Excipient

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

Class III — Low RiskTerminated
Refund
October 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets

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

Class II — Potential Health HazardTerminated
Refund
October 6, 2016· Actavis Elizabeth LLC

Recalled Item: NIFEdipine Capsules USP

The Issue: Presence of Foreign Tablets/Capsules

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

Class III — Low RiskTerminated
Refund
October 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets

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

Class II — Potential Health HazardTerminated
Refund
October 5, 2016· Par Pharmaceutical, Inc.

Recalled Item: Travoprost Ophthalmic Solution USP

The Issue: Lack of Assurance of Sterility; damage to the

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

Class II — Potential Health HazardTerminated
Refund
October 3, 2016· West-Ward Pharmaceutical

Recalled Item: PredniSONE Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 3, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Phenobarbital Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
September 30, 2016· Amerisource Health Services

Recalled Item: Paricalcitol Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
September 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
September 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
September 27, 2016· North American Rescue LLC.

Recalled Item: Range Trauma Kit - Product Code 85-1274

The Issue: Lack of Assurance of Sterility: Concerns with product

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess FE 1/20 (norethindrone acetate

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskCompleted
Refund
September 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1.5/30 (norethindrone acetate

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskCompleted
Refund
September 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1/20 (norethindrone acetate

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskCompleted
Refund
September 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess FE 1.5/30 (norethindrone acetate

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskCompleted
Refund
September 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 24 FE 1.5/30 (norethindrone acetate

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskCompleted
Refund