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 17441–17460 of 17,529 recalls

May 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Octreotide Acetate Injection

The Issue: Short Fill: These products are being recalled because

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

Class II — Potential Health HazardTerminated
Refund
April 30, 2012· Apotex Inc.

Recalled Item: Dorzolamide HCI/Timolol Maleate Ophthalmic Solution 22.3mg/6.8mg per mL

The Issue: Presence of Particulate Matter: Lots identified in this

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

Class II — Potential Health HazardTerminated
Refund
April 26, 2012· Bayer Healthcare, LLC

Recalled Item: Midol Complete

The Issue: Labeling: Label Mix-up: This recall was initiated after

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

Class III — Low RiskTerminated
Refund
April 26, 2012· Bayer Healthcare, LLC

Recalled Item: Midol Complete

The Issue: Labeling: Label Mix-up: This recall was initiated after

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

Class III — Low RiskTerminated
Refund
April 24, 2012· Luitpold Pharmaceuticals, Inc.

Recalled Item: Epinephrine Injection

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: CABERGOLINE Tablets

The Issue: Impurities/Degradation Products: This lot of product will not

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

Class III — Low RiskTerminated
Refund
April 23, 2012· Carefusion 213, Llc

Recalled Item: ChloraPrep One-Step (2% w/v chlorhexidine gluconate and 70% v/v isopropyl

The Issue: Lack of Assurance of Sterility: Firm mistakenly released

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

Class II — Potential Health HazardTerminated
Refund
April 23, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa (levonorgestrel/ethinyl estradiol tablets

The Issue: Contraceptive Tablets Out of Sequence: This recall has

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

Class III — Low RiskTerminated
Refund
April 21, 2012· XRock Industries, LLC

Recalled Item: X-ROCK For Men

The Issue: Marketed Without an Approved NDA/ANDA: product tested positive

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

Class I — Serious Health HazardTerminated
Refund
April 17, 2012· Watson Laboratories Inc

Recalled Item: Loxapine Capsules USP

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated

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

Class III — Low RiskTerminated
Refund
April 17, 2012· Watson Laboratories Inc

Recalled Item: Loxitane Capsules

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated

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

Class III — Low RiskTerminated
Refund
April 17, 2012· Watson Laboratories Inc

Recalled Item: Loxapine Capsules USP

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated

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

Class III — Low RiskTerminated
Refund
April 17, 2012· Hospira Inc.

Recalled Item: Morphine Sulfate Injection

The Issue: Superpotent; Cartridges labeled to contain 1 mL found

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

Class I — Serious Health HazardTerminated
Refund
April 17, 2012· Watson Laboratories Inc

Recalled Item: Loxapine Capsules USP

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated

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

Class III — Low RiskTerminated
Refund
April 17, 2012· Watson Laboratories Inc

Recalled Item: Loxapine Capsules USP

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated

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

Class III — Low RiskTerminated
Refund
April 16, 2012· Bracco Diagnostics Inc

Recalled Item: Multihance Multipack (gadobenate dimeglumine) injection

The Issue: Lack of Assurance of Sterility; Product recalled due

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

Class II — Potential Health HazardTerminated
Refund
April 16, 2012· Bracco Diagnostics Inc

Recalled Item: Bracco Diagnostics multihance (gadobenate dimeglumine) injection

The Issue: Short Fill: The product is being recalled due

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

Class III — Low RiskTerminated
Refund
April 13, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Fosphenytoin Sodium Injection

The Issue: Presence of Particulate Matter: This product is being

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

Class II — Potential Health HazardTerminated
Refund
April 13, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Fosphenytoin Sodium Injection

The Issue: Presence of Particulate Matter: This product is being

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

Class II — Potential Health HazardTerminated
Refund
April 11, 2012· Hospira, Inc.

Recalled Item: Propofol Injectable Emulsion

The Issue: Presence of Particulate Matter: A single visible particulate

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

Class II — Potential Health HazardTerminated
Refund