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 13421–13440 of 17,529 recalls

March 10, 2015· the Compounder

Recalled Item: BIEST CP 76/24: DHEA (Estriol USP Micronized (E3)/Estradiol (E2) Trit

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 67/33 (Estradiol (E2) TRIT (YELLOW)/Estriol USP Micronized (E3))

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) 4.0MG capsules

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3))

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 MG/ML

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG :

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 86/14 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (yellow) / Estriol USP

The Issue: Recalled products were made using an active ingredient

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2015· Freedom Pharmaceuticals Inc

Recalled Item: Domperidone BP

The Issue: Penicillin Cross Contamination: Potential for products to be

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

Class II — Potential Health HazardTerminated
Refund
March 9, 2015· Navinta LLC

Recalled Item: Fomepizole 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
March 6, 2015· Fusion Pharmaceuticals, LLC

Recalled Item: DICOPANOL (diphenhydramine hydrochloride in 5 mg/mL oral suspension kit) FusePaq

The Issue: Microbial Contamination of a Non-Sterile Product: Kit component

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

Class II — Potential Health HazardTerminated
Refund
March 6, 2015· Hospira Inc.

Recalled Item: MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION

The Issue: Mislabeling

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

Class I — Serious Health HazardTerminated
Refund
March 5, 2015· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Presence of Particulate Matter: Confirmed finding of human

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

Class I — Serious Health HazardTerminated
Refund
March 5, 2015· Hospira Inc.

Recalled Item: 5% DEXTROSE Injection

The Issue: Lack of Assurance of Sterility: there is a

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

Class II — Potential Health HazardTerminated
Refund
March 2, 2015· American Health Packaging

Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 2, 2015· Safecor Health, LLC

Recalled Item: Haloperidol Oral Solution

The Issue: Defective Container: Confirmed customer complaints of leaking bottles

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

Class II — Potential Health HazardTerminated
Refund