the Compounder recalls BIEST TD 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) : PROGESTERONE W/V (weight/volume) PLO (Pluroni
Recalled November 18, 2015 · FDA recall D-0212-2016 · the Compounder
Hazard
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. · FDA Class II
Units
10 (10mL) syringes
Sold at
Nationwide
Description
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Product
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.
Manufacturer(s)
the Compounder
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →