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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 12,901–12,920 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) W/V (weight/volume) 1.25:100:0.625 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only,The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) W/V (weight/volume) 5.0 :20 :1 MG/ML Transdermal cream, dispensed in 5 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : TESTO (Testosterone USP) : DHEA (Dehydroepiandrosterone Micronized) W/V (weight/volume) VERSABASE 2.5 : 17.5 : 1.25 :0.25MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only,The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) IN VERSABASE W/V (weight/volume) 4 : 67.5 :10MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) IN VERSABASE W/V (weight/volume) 2.5 : 25 :1.25MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 6.5 : 30: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 3: 25: 1.25: 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) 2.5 : 20 : 1.25 : 0.25 MG/ML TRANSDERMAL (Cream)Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized) : DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 5.0 : 30 : 2.5 : 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : PROG (Progesterone USP Micronized): DHEA (Dehydroepiandrosterone Micronized) : TESTO (Testosterone Trit) W/V (weight/volume) VERSABASE 2.5: 30 : 2.5 : 0.25 MG/MLTransdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (yellow) / Estriol USP Micronized (E3)): PROG (Progesterone USP Micronized) W/V 2.5MG:100MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) W/V(weight/volume) [2977] 6.25MG/ML Transdermal cream, dispensed in 1 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) W/V (weight/volume) 5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)) W/V (weight/volume) 2.5MG/ML Transdermal cream, dispensed in a) 3 mL and b) 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 12.5 MG/ML 1.25MG/0.1ML Transdermal cream, dispensed in 1 mL prefilled, amber syringes,Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 0.25 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 8 MG/ML transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 67/33 (Estradiol (E2) TRIT (YELLOW)/Estriol USP Micronized (E3)) W/V (weight /volume) 1.5 MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 4.0 MG/ML transdermal cream packaged in 3mL syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cream, dispensed in 10 mL prefilled syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

by the Compounder

Reason
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recall initiated
March 10, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.