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 15921–15940 of 17,529 recalls

June 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskTerminated
Refund
June 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Nata Komplete

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskTerminated
Refund
June 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: NataChew

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskTerminated
Refund
June 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskTerminated
Refund
June 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 ec

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskTerminated
Refund
June 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Clalis capsules

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
June 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint

The Issue: Subpotent drug: Avobenzone 3%, one of the active

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

Class III — Low RiskTerminated
Refund
June 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint

The Issue: Subpotent Drug: Avobenzone 3%, one of the active

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

Class III — Low RiskTerminated
Refund
June 27, 2013· Hospira Inc.

Recalled Item: Sodium Chloride Injection

The Issue: Presence of Particulate Matter: Confirmed customer report of

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

Class II — Potential Health HazardTerminated
Refund
June 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint

The Issue: Subpotent Drug: Avobenzone 3%, one of the active

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

Class III — Low RiskTerminated
Refund
June 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Silver Sword capsules

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
June 25, 2013· Apotex Inc

Recalled Item: Latanoprost Ophthalmic Solution

The Issue: Lack of Assurance of Sterility: Failed at expiry

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

Class II — Potential Health HazardTerminated
Refund
June 24, 2013· Fresenius Kabi USA, LLC

Recalled Item: Oxytocin Injection

The Issue: Subpotent Drug; 15-month stability test station

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

Class II — Potential Health HazardTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: GIRLS ROCK Justice

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: Share a Smile Mixed berry Anti bac Justice

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: I love my BFF Justice

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: YOU CANT HANDLE THIS Justice

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: I love to shop Justice

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: Shine from within blueberry Anti bac Justice

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund
June 21, 2013· Tween Brands Inc

Recalled Item: Girls can change the World

The Issue: Labeling: Label Error on Declared Strength; the label

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

Class III — Low RiskTerminated
Refund