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 14841–14860 of 17,529 recalls

January 15, 2014· Watson Laboratories Inc

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 14, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Levothyroxine Sodium Tablets

The Issue: Subpotent Drug: Assay results obtained during stability testing

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

Class II — Potential Health HazardTerminated
Refund
January 14, 2014· Traxx International Corp

Recalled Item: Guaifenesin USP

The Issue: Presence of Foreign Matter: Guaifenesin API powder is

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

Class II — Potential Health HazardTerminated
Refund
January 13, 2014· HUMAN SCIENCE FOUNDATION

Recalled Item: PRO ArthMax Dietary Supplement tablets

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found

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

Class I — Serious Health HazardTerminated
Refund
January 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets

The Issue: Defective Container; some of the outer laminate foil

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

Class III — Low RiskTerminated
Refund
January 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets

The Issue: This recall of LIPTRUZET is being initiated due

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

Class III — Low RiskTerminated
Refund
January 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets

The Issue: This recall of LIPTRUZET is being initiated due

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

Class III — Low RiskTerminated
Refund
January 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets

The Issue: This recall of LIPTRUZET is being initiated due

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

Class III — Low RiskTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Cream 2 oz. containers in the

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion which was...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Baby's Relief Calm and Repair Cream in 2 oz.

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Hospira Inc.

Recalled Item: DOBUTamine Injection

The Issue: Presence of Particulate Matter: Discolored solution due to

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

Class I — Serious Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020.

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Serum

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2014· Dermamedics, L.L.C.

Recalled Item: Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
January 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: Magic For Men

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
January 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: ExtenZe 600 mg

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund