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 13241–13260 of 17,529 recalls

May 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets

The Issue: Subpotent drug

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

Class III — Low RiskTerminated
Refund
May 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets

The Issue: Subpotent drug

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

Class III — Low RiskTerminated
Refund
May 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets

The Issue: Subpotent drug

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

Class III — Low RiskTerminated
Refund
May 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets

The Issue: Subpotent drug

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

Class III — Low RiskTerminated
Refund
May 4, 2015· Ohm Laboratories, Inc.

Recalled Item: 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
April 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP

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

Class II — Potential Health HazardTerminated
Refund
April 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP

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

Class II — Potential Health HazardTerminated
Refund
April 29, 2015· Janssen Pharmaceuticals, Inc.

Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
April 29, 2015· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Azithromycin 500 mg tablets

The Issue: cGMP Deviations: This recall is a result of

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

Class II — Potential Health HazardTerminated
Refund
April 29, 2015· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Azithromycin Tablets

The Issue: cGMP Deviations: This recall is a result of

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

Class II — Potential Health HazardTerminated
Refund
April 28, 2015· Teva Pharmaceuticals USA

Recalled Item: Adrucil (fluorouracil injection

The Issue: Presence of Particulate Matter: Black particulate matter was

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

Class I — Serious Health HazardTerminated
Refund
April 28, 2015· Fresenius Kabi USA, LLC

Recalled Item: KABIVEN [(3.9%) Lipid Injectable Emulsion with (3.1%) Amino Acids and

The Issue: Labeling: Label Error on Declared Strength: Labeled 3.1%

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

Class II — Potential Health HazardTerminated
Refund
April 28, 2015· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCl 50 mg in 0.9% Sodium Chloride 250 mL

The Issue: Labeling: Label Mix-Up: Product is incorrectly labeled as

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2015· Cipla Limited

Recalled Item: Levalbuterol Inhalation Solution

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
April 24, 2015· Romark Laboratories, L.C.

Recalled Item: Alinia (nitazoxanide)

The Issue: Failed Stability Specifications: Product failed to meet 12

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

Class II — Potential Health HazardTerminated
Refund
April 23, 2015· South Coast Specialty Compounding, Inc.

Recalled Item: Estradiol

The Issue: Penicillin Cross Contamination: Multiple finished products potentially contamina

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

Class II — Potential Health HazardTerminated
Refund
April 23, 2015· Mylan Institutional LLC

Recalled Item: Cytarabine Injection 100 mg/5 mL (20 mg/mL)

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardTerminated
Refund
April 23, 2015· Hospira Inc.

Recalled Item: Bupivacaine Hydrochloride Inj.

The Issue: Presence of Particulate Matter: Presence of free-floating and

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

Class I — Serious Health HazardTerminated
Refund
April 23, 2015· South Coast Specialty Compounding, Inc.

Recalled Item: Bi-Est (estriol

The Issue: Penicillin Cross Contamination: Multiple finished products potentially contamina

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

Class II — Potential Health HazardTerminated
Refund
April 23, 2015· South Coast Specialty Compounding, Inc.

Recalled Item: Tri-Est 80:10:10 Progesterone (estriol

The Issue: Penicillin Cross Contamination: Multiple finished products potentially contamina

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

Class II — Potential Health HazardTerminated
Refund