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 10641–10660 of 17,529 recalls

December 20, 2016· Accord Healthcare, Inc.

Recalled Item: Lisinopril tablets

The Issue: Failed tablet/capsule specification: missing break line on the

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

Class II — Potential Health HazardTerminated
Refund
December 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
December 20, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
December 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 20, 2016· Mylan LLC.

Recalled Item: Temozolomide Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 19, 2016· Apotex Inc.

Recalled Item: Aripiprazole Tablets

The Issue: Superpotent Drug: Product may not meet specifications throughout

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

Class III — Low RiskTerminated
Refund
December 16, 2016· Aurobindo Pharma USA Inc

Recalled Item: Pantoprazole Sodium for Injection

The Issue: Discoloration: Some vials were found to contain powder

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

Class III — Low RiskTerminated
Refund
December 16, 2016· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM INJECTION

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 15, 2016· Gentell, Inc

Recalled Item: Gentell Hydrogel Wound Dressing REGULAR

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
December 15, 2016· Gentell, Inc

Recalled Item: Gentell Hydrogel Ag Saturated Gauze

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
December 15, 2016· Amgen, Inc.

Recalled Item: AMGEN Kyprolis (carfilzomib) for injection

The Issue: Lack of Assurance of Sterility: Potential cracks in

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

Class II — Potential Health HazardTerminated
Refund
December 15, 2016· Meta Pharmacy Services

Recalled Item: Phenylephrine 2.5% + Tropicamide 1% Compounded Eye Drops Solution

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardTerminated
Refund
December 14, 2016· Roxane Laboratories, Inc.

Recalled Item: Azelastine Hydrochloride Nasal Solution (Nasal Spray)

The Issue: Defective Delivery System: out of specification result for

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

Class III — Low RiskTerminated
Refund
December 14, 2016· Apotex Corp.

Recalled Item: Torsemide Tablets

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
December 14, 2016· Apotex Corp.

Recalled Item: Torsemide Tablets

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
December 13, 2016· Pacific Medical Solutions

Recalled Item: Nano PNC Water

The Issue: Marketed without an Approved NDA/ANDA and non-sterility: NANO

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

Class I — Serious Health HazardTerminated
Refund
December 13, 2016· Sandoz Inc

Recalled Item: Donepezil Hydrochloride Tablets

The Issue: Subpotent Drug: out of specification results for assay

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

Class III — Low RiskTerminated
Refund
December 12, 2016· Amneal Pharmaceuticals LLC

Recalled Item: Rabeprazole Sodium Delayed Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund