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
1 this month

Showing 6601–6620 of 17,529 recalls

August 23, 2019· Aurolife Pharma, LLC

Recalled Item: fexofenadine hydrochloride tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine HCL Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (fexofenadine hydrochrloride) tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochrloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine HCl) tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 21, 2019· Macleods Pharma Usa Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg

The Issue: Subpotent Drug: Out of specification result during stability

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

Class III — Low RiskTerminated
Refund
August 16, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 14, 2019· Pfizer Inc.

Recalled Item: RELPAX (eletriptan HBr) tablets

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

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

Class II — Potential Health HazardTerminated
Refund
August 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-GLUTATHIONE 200MG/3ML (PF) INHALATION SOLN

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-PYRIDOXINE HCL (B6) 100MG/ML MDV

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-TEST CYP/PROP/DECA-NAN 250MG/ML (80/10/10) IN SESAME OIL

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-HYDROGEN PEROXIDE 3% (PF) 30ML glass vial

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-PROCAINE HCL 1% BUFFERED MDV

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-CALM INJECTION

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund