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 13381–13400 of 17,529 recalls

March 11, 2015· Hospira Inc.

Recalled Item: LACTATED RINGER'S IRRIGATION

The Issue: Non-Sterility: Confirmed customer report of dark, fibrous particulates

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

Class I — Serious Health HazardTerminated
Refund
March 11, 2015· Mylan Pharmaceuticals Inc.

Recalled Item: Fexofenadine HCl Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 10, 2015· Matheson, Inc.

Recalled Item: AIR COMPRESSED

The Issue: Failed Impurities/Degradation Specification; out of specification results for

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

Class III — Low RiskTerminated
Refund
March 10, 2015· Mutual Pharmaceutical Company, Inc.

Recalled Item: Ergoloid Mesylates

The Issue: Failed Quality Specifications

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: BIEST TD 83/17 (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) W/V (weight/volume) PGF 0.1% (1.0MG/ML) Transdermal cream

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 50/50 (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) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) :

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 CP 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 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow))

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 : DHEA (Dehydroepiandrosterone Micronized) W/V...

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 CP 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) W/V (weight/volume) VERSABASE 3MG/ML Transdermal cream

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: 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: 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