the Compounder recalls BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cr
Recalled November 18, 2015 · FDA recall D-0187-2016 · 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
3 (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 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cream, dispensed in 10 mL prefilled 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 →