D-0192-2016 Class II Terminated

Recalled by the Compounder — Aurora, IL

Recall Details

Product Type
Drugs
Report Date
November 18, 2015
Initiation Date
March 10, 2015
Termination Date
May 19, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
9 (1mL) syringes

Product Description

BIEST TD 80/20 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 12.5 MG/ML 1.25MG/0.1ML Transdermal cream, dispensed in 1 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 Pattern

Nationwide

Code Information

Lot # 01232015:17@35, Exp 8/11/2015