# FDA recall D-0194-2016

> **the Compounder** · Class II · drug recall initiated 2015-03-10.

## Product

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.

## Reason for recall

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0194-2016
- **Recalling firm:** the Compounder
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-03-10
- **Report date:** 2015-11-18
- **Termination date:** 2016-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Aurora, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0194-2016

## Citation

> AI Analytics. FDA recall D-0194-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0194-2016. Source: US FDA. Licensed CC0.

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