RecallRadar

FDA Drug recall D-0220-2016

ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, R…

On 2015-11-18 the FDA classified a Class II recall of ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, R… by The Compounder, citing recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0220-2016
ClassificationClass II
Statusterminated
Initiated2015-03-10
Published2015-11-18
Last updated2026-09-13 11:51 UTC
CompanyThe Compounder
DistributionUS

Product

ESTRIOL (E3) : TESTO (Testosterone USP) WV (weight/volume) 0.5MG : 2MG/ML Transdermal cream, dispensed in 3 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

Reason

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Identifiers

code_infoLot # 12292014:45@12, Exp 6/27/2015; Lot # 01282015:06@16, Exp 7/27/2015; Lot # 03022015:06@38, Exp 8/29/2015

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0220-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.