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 11001–11020 of 17,529 recalls

August 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate

The Issue: Unit Dose Mispackaging; blister cavities may contain more

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

Class II — Potential Health HazardTerminated
Refund
August 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate

The Issue: Unit Dose Mispackaging; blister cavities may contain more

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

Class II — Potential Health HazardTerminated
Refund
August 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate

The Issue: Unit Dose Mispackaging; blister cavities may contain more

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

Class II — Potential Health HazardTerminated
Refund
August 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate

The Issue: Unit Dose Mispackaging; blister cavities may contain more

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

Class II — Potential Health HazardTerminated
Refund
August 24, 2016· Sandoz Inc

Recalled Item: Phenylephrine HCI Injection

The Issue: Lack of Assurance of Sterility: a recent FDA

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

Class II — Potential Health HazardTerminated
Refund
August 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate

The Issue: Unit Dose Mispackaging; blister cavities may contain more

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2016· Stason Pharmaceuticals, Inc.

Recalled Item: Selegiline HCL Tablets USP 5mg

The Issue: Stason Pharmaceuticals is recalling Selegiline HCl tablets, USP

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

Class III — Low RiskTerminated
Refund
August 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch

The Issue: Defective Delivery System: Out of Specification (OOS) results

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

Class II — Potential Health HazardTerminated
Refund
August 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch

The Issue: Defective Delivery System: Out of Specification (OOS) results

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

Class II — Potential Health HazardTerminated
Refund
August 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch

The Issue: Defective Delivery System: Out of Specification (OOS) results

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

Class II — Potential Health HazardTerminated
Refund
August 19, 2016· Unichem Pharmaceuticals Usa Inc

Recalled Item: Lamotrigine Tablets

The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed

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

Class III — Low RiskTerminated
Refund
August 19, 2016· Impax Laboratories, Inc.

Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT)

The Issue: Labeling; Label Mixup; box labeled to contain 200

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

Class I — Serious Health HazardTerminated
Refund
August 18, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Amoxicillin For Oral Suspension

The Issue: Labeling: Label Error on Declared Strength- bottles missing

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

Class III — Low RiskTerminated
Refund
August 16, 2016· Sperian Eye & Face Protection, Inc

Recalled Item: Honeywell eyesaline Eyewash Sterile Isotonic Solution

The Issue: Non Sterility; contaminated with Klebsiella pneumoniae

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

Class I — Serious Health HazardTerminated
Refund
August 15, 2016· Hospira Inc.

Recalled Item: DOBUTamine Injection

The Issue: Discoloration: Firm received complaints of product discoloration and

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2016· Allergy Laboratories, Inc.

Recalled Item: Ephedrine Sulfate Injection

The Issue: Lack of Assurance of Sterility: An FDA inspection

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid

The Issue: CGMP Deviations: Recall initiated as a precautionary measure

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2016· Pharmatech LLC

Recalled Item: Senexon Liquid (sennosides) 8.8 mg

The Issue: CGMP Deviations: Recall initiated as a precautionary measure

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2016· Pharmatech LLC

Recalled Item: Sennazon (sennosides) Syrup

The Issue: CGMP Deviations: Recall initiated as a precautionary measure

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2016· Pharmatech LLC

Recalled Item: Diocto Syrup (docusate sodium)

The Issue: CGMP Deviations: Recall initiated as a precautionary measure

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

Class II — Potential Health HazardTerminated
Refund