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 11721–11740 of 17,529 recalls

February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 10 mg/ml/Baclofen 460 mcg/ml/Bupivacaine HCL

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Morphine Sulfate 0.5 mg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Morphine Sulfate 10 mg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 10 mg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 20 mg/ml/Bupivacaine HCL 40 mg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Fentanyl Citrate 1.275 mg/ml/Baclofen 150 mcg/ml/Bupivacaine HCL 20 mg/ml/...

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Sufentanil Cit 50 mcg/ml/Clonidine HCL 1 mcg/ml/Bupivacaine HCL 5 mg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 7 mg/ml/Bupivacaine HCL 11.2 mg/ml

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
February 2, 2016· Hospira Inc.

Recalled Item: Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) 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 RiskOngoing
Refund
February 2, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone Diacetate Injectable Suspension

The Issue: Mislabeling

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

Class III — Low RiskTerminated
Refund
January 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
January 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 40 mg

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 27, 2016· Bonita Pharmaceuticals, LLC

Recalled Item: Menthocin Patch with Lidocaine-Strong (Menthol 5%

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
January 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 80 mg

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 20 mg

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 10 mg

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules

The Issue: Failed Dissolution Specification: Out of specification dissolution results

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

Class III — Low RiskTerminated
Refund
January 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules

The Issue: Failed Dissolution Specification: Out of specification dissolution results

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

Class III — Low RiskTerminated
Refund
January 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules

The Issue: Failed Dissolution Specification: Out of specification dissolution results

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

Class III — Low RiskTerminated
Refund