the Compounder recalls BIEST TD 80/20 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow)) W/V(weight/volume) [2977] 6.25MG/ML Transderm
Recalled November 18, 2015 · FDA recall D-0195-2016 · 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
36 (1 mL) 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 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.
Manufacturer(s)
the Compounder
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →