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 14721–14740 of 17,529 recalls

March 18, 2014· Glenmark Generics Inc., USA

Recalled Item: Ranitidine Tablets USP

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 17, 2014· John W Hollis Inc

Recalled Item: Papaverine 60 mg

The Issue: Labeling: Incorrect Expiration Date; Expiration date is earlier

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

Class III — Low RiskTerminated
Refund
March 17, 2014· John W Hollis Inc

Recalled Item: Phosphatidylcholine Solution for Injection

The Issue: Labeling: Incorrect Expiration Date; Expiration date is earlier

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

Class II — Potential Health HazardTerminated
Refund
March 17, 2014· John W Hollis Inc

Recalled Item: Polidocanol 1% Solution

The Issue: Labeling: Incorrect Expiration Date; Expiration date is earlier

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

Class III — Low RiskTerminated
Refund
March 17, 2014· John W Hollis Inc

Recalled Item: Polidocanol 3% Solution

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardTerminated
Refund
March 14, 2014· Shire Human Genetic Therapies, Inc.

Recalled Item: VPRIV¿ (velaglucerase alfa for injection)

The Issue: Presence of Particulate Matter; Particulates identified as stainless

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

Class I — Serious Health HazardTerminated
Refund
March 13, 2014· Pain Free By Nature

Recalled Item: REUMOFAN PLUS Tablets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardTerminated
Refund
March 13, 2014· Blu Pharmaceuticals Inc

Recalled Item: Metformin Hydrochloride Tablets USP 500 mg

The Issue: Defective container: Product distributed without inner seal on

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

Class II — Potential Health HazardTerminated
Refund
March 13, 2014· Blu Pharmaceuticals Inc

Recalled Item: Metformin Hydrochloride Tablets USP 1000 mg

The Issue: Defective container: Product distributed without inner seal on

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

Class II — Potential Health HazardTerminated
Refund
March 11, 2014· Paddock Laboratories, LLC

Recalled Item: Perrigo

The Issue: Presence of Particulate Matter Perrigo is recalling seven

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (leuprolide acetate for depot suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2014· AbbVie Inc

Recalled Item: LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may

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

Class II — Potential Health HazardTerminated
Refund
March 6, 2014· Greenstone Llc

Recalled Item: Venlafaxine HCl Extended-Release Capsules

The Issue: Presence of Foreign Tablets/Capsules: report of a foreign

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

Class I — Serious Health HazardTerminated
Refund
March 6, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Effexor XR (venlafaxine HCl) Extended-Release Capsules

The Issue: Presence of Foreign Tablets/Capsules: A Pharmacist reported that

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

Class I — Serious Health HazardTerminated
Refund
March 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund