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 11021–11040 of 17,529 recalls

August 8, 2016· Pharmatech LLC

Recalled Item: Senna Syrup (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: Ninjacof-A (acetaminophen

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: Aller-Chlor (chlorpheniramine maleate) 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 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP)

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 4, 2016· Amerisource Health Services

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 4, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Bupivacaine Hydrochloride Inj.

The Issue: Presence of particulate matter: Confirmed customer report for

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

Class I — Serious Health HazardOngoing
Refund
August 4, 2016· Genzyme Corporation / Genzyme Biosurgery

Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskTerminated
Refund
August 3, 2016· Golden State Medical Supply Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-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
August 3, 2016· Aurobindo Pharma USA Inc

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets USP

The Issue: Presence of Foreign Tablets/Capsules: Firm received a market

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

Class II — Potential Health HazardTerminated
Refund
August 3, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 3, 2016· Golden State Medical Supply Inc.

Recalled Item: Venlafaxine Hydrochloride Extended-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
August 3, 2016· Reckitt Benckiser LLC

Recalled Item: Mucinex Sinus-Max Day Night

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

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

Class III — Low RiskTerminated
Refund
August 2, 2016· Actavis Inc

Recalled Item: Acetasol HC (hydrocortisone and acetic acid otic solution USP)

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 2, 2016· Actavis Inc

Recalled Item: Hydrocortisone and acetic acid otic solution

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 1, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension

The Issue: Lack of processing controls: Isomeric Pharmacy Solution, LLC

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

Class II — Potential Health HazardTerminated
Refund
August 1, 2016· Spectrum Laboratory Products, Inc.

Recalled Item: Zinc Acetate

The Issue: Does not meet monograph: product exhibits lead levels

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

Class II — Potential Health HazardTerminated
Refund
August 1, 2016· Town and Country Compounding and Consultation Services

Recalled Item: Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I

The Issue: Non-Sterility; microbial contamination identified as Bacillus circulans

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

Class I — Serious Health HazardTerminated
Refund
July 29, 2016· Teva Pharmaceuticals USA

Recalled Item: Amikacin Sulfate Injection

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
July 29, 2016· Sage Products LLC

Recalled Item: COMFORT SHIELD (dimethicone) Barrier Cream Cloths

The Issue: CGMP Deviations: potential contamination of products manufactured on

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

Class II — Potential Health HazardTerminated
Refund
July 29, 2016· Sage Products LLC

Recalled Item: COMFORT SHIELD (dimethicone) Barrier Cream Cloths

The Issue: Microbial Contamination of Non-Sterile Products: contamination with the

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

Class I — Serious Health HazardTerminated
Refund