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 9681–9700 of 17,529 recalls

October 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Midazolam HCL 100 mg (1mg/mL) 100 mL Cassette in 0.9% Sodium Chloride

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: fentanyl citrate (PF) 1100 mcg (20 mcg/mL) 55 mL syringes

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Succinylcholine 200 mg/10 mL Syringe

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 6, 2017· NEW RELIANCE TRADING, INC.

Recalled Item: No.1 Faiza Beauty Cream Manufactured by: Poonia Brothers (Pak)

The Issue: Marketed Without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 6, 2017· AVKARE Inc.

Recalled Item: Duloxetine Delayed-release Capsules 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 6, 2017· Kiriko, LLC.

Recalled Item: A1 Slim

The Issue: Undeclared Sibutramine

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

Class II — Potential Health HazardTerminated
Refund
October 5, 2017· Purdue Pharma, LP

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP

The Issue: Subpotent Drug: The laminate used to make the

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

Class II — Potential Health HazardTerminated
Refund
October 3, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Famotidine tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 2, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Bisoprolol Fumarate 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 28, 2017· Leading Pharma, LLC

Recalled Item: Lorazepam Tablets

The Issue: Labeling: Label Error on Declared Strength. Bottle labeled

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2017· Pfizer Manufacturing Deutschland GmbH

Recalled Item: FOR EXPORT ONLY Atorvastatin calcium Film-Coated Tablets a) 80 mg SMT Tabs Bulk

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2017· United Pharmacy

Recalled Item: Glutamine

The Issue: CGMP Deviations; FDA analysis deterrmined that the product

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

Class II — Potential Health HazardTerminated
Refund
September 26, 2017· Pharmedium Services, LLC

Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in

The Issue: Superpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskTerminated
Refund
September 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskTerminated
Refund
September 26, 2017· Pharmedium Services, LLC

Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskTerminated
Refund
September 26, 2017· The Harvard Drug Group

Recalled Item: Alprazolam 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 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets

The Issue: Subpotent Drug: Out of specification assay result in

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

Class III — Low RiskTerminated
Refund
September 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets

The Issue: Subpotent Drug: Out of specification assay result in

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

Class III — Low RiskTerminated
Refund
September 25, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension USP

The Issue: Subpotent Drug: low out of specification results

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

Class III — Low RiskTerminated
Refund