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 9121–9140 of 17,529 recalls

April 24, 2018· Prescript Pharmaceuticals, Inc.

Recalled Item: Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets

The Issue: Labeling: Not Elsewhere Classified: due to a labeled

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Prescript Pharmaceuticals, Inc.

Recalled Item: Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets

The Issue: Labeling: Not Elsewhere Classified: due to a labeled

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine and Benazapril HCL Capsules

The Issue: cGMP Deviations; cleaning processes for equipment used to

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Prescript Pharmaceuticals, Inc.

Recalled Item: Chlorhexidine 0.12% liquid

The Issue: Labeling: Not Elsewhere Classified: due to a labeled

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Prescript Pharmaceuticals, Inc.

Recalled Item: Clindamycin 150 mg capsules

The Issue: Labeling: Not Elsewhere Classified: due to a labeled

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Prescript Pharmaceuticals, Inc.

Recalled Item: Clindamycin 300 mg capsules

The Issue: Labeling: Not Elsewhere Classified: due to a labeled

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Vitalab Pharmacy, Inc

Recalled Item: Methylcobalamin for injection

The Issue: Lack of assurance of sterility: Upon review of

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Vitalab Pharmacy, Inc

Recalled Item: Papaverine 30mg/Phentolamine 1.5mg/Prostaglandin 50mcg/mL

The Issue: Lack of assurance of sterility: Upon review of

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Vitalab Pharmacy, Inc

Recalled Item: Methionine 25mg/Inositol 50mg/Choline 50mg/Cyanocobalamin 1mg/ml

The Issue: Lack of assurance of sterility: Upon review of

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Vitalab Pharmacy, Inc

Recalled Item: Papaverine 9mg/Phentolamine 1mg/Atropine 0.1mg/Prostaglandinl 10mcg/ml

The Issue: Lack of assurance of sterility: Upon review of

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Vitalab Pharmacy, Inc

Recalled Item: Papaverine 30mg/Phentolamine 2mg/Prostaglandin 20mcg/mL

The Issue: Lack of assurance of sterility: Upon review of

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2018· Vitalab Pharmacy, Inc

Recalled Item: Alprostadil 20 mcg/mL

The Issue: Lack of assurance of sterility: Upon review of

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

Class II — Potential Health HazardTerminated
Refund
April 23, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets

The Issue: Presence of Foreign Tablets/Capsules: One foreign tablet identified

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

Class II — Potential Health HazardTerminated
Refund
April 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
April 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
April 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
April 20, 2018· Exela Pharma Sciences LLC

Recalled Item: Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg

The Issue: Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium

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

Class II — Potential Health HazardTerminated
Refund
April 19, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets USP

The Issue: Presence of Foreign Substance:Sun Pharma is recalling one

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

Class II — Potential Health HazardTerminated
Refund
April 17, 2018· Rhodes Pharmaceuticals, L.P.

Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only

The Issue: Failed Dissolution Specification: Low dissolution outside of specifications

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

Class III — Low RiskTerminated
Refund
April 16, 2018· Epic Products, LLC

Recalled Item: Euphoric Premium Male Performance Enhancer capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund