the Compounder recalls BIEST TD 83/17 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3) W/V (weight/volume) 1.2 MG/ML Transdermal crea
Recalled November 18, 2015 · FDA recall D-0209-2016 · 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
6 (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 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.
Manufacturer(s)
the Compounder
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →