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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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Drug Recall Terminated Historical recordClass II

TRIEST 70/20/10 ( Estriol USP / Estradiol USP (E2) / Estrone (E1) Triturate) [909] 12.5MG/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

ESTRIOL 5 ESTRADIOL (Estradiol (E2) Trit (Yellow)) 0.95 ESTRONE (Estrone E1) Trit (Red)) 0.02 TEST (Testosterone USP) 0.75MG/ML W/V (weight/volume) 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

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Drug Recall Terminated Historical recordClass II

ESTRIOL (E3) W/V (weight/volume) VERSABASE [4714] 0.05% (0.5MG/ML) transdermal cream, dispensed in a) 1 mL and b) 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

ESTRIOL (E3) W/V (weight/volume) VERSABASE 3MG/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

ESTRIOL (E3) W/V (weight/volume) PGF 0.1% (1.0MG/ML) Transdermal cream, is 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

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Drug Recall Terminated Historical recordClass II

ESTRIOL (E3) 2.5MG suppositories, 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

ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/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

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : TESTO (Testosterone USP) W/V (weight/volume) 2.0: 0.1: 0.5MG/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

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 30 : 0.5 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

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 35 : 0.5 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

ESTRIOL (E3) : PROGESTERONE W/V (weight/volume) 4.0 : 100 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

ESTRIOL (E3) : PROGESTERONE : DHEA (Dehydroepiandrosterone Micronized) W/V (weight/volume) VERSABASE 4.0 : 30 : 4MG/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

ESTRIOL (E3) 4.0MG capsules, 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

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Drug Recall Terminated Historical recordClass II

E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized (E3) : PROGEST (Progesterone USP Micronized) : TESTOST (Testosterone USP) IN OLIVE OIL 0.75 : 3 : 50 : 5MG capsules, 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 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) : PROGESTERONE W/V (weight/volume) PLO (Pluronic F127 20% or Polox 20% gel) 3.3 MG/ML : 40 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 89/11 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) VERSABASE 2.25MG/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 86/14 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) IN PLO GEL (Pluronic F127 20% or Polox 20% gel) 2.9 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 83/17 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) 1.2 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) VAN CR (vanishing cream) W/V (weight/volume) (4812) 2.5MG/ML Transdermal cream, dispensed in a) 1mL and b)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 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) : TESTO (Testosterone USP) W/V (weight/volume) 1.0 :4.0 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 →

Data last updated: September 27, 2026 ET

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.