FDA Drug Recalls

Recalls / Class II

Class IID-0183-2016

Product

BIEST 80/20 : PROGEST : DHEA : TESTOST (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow): Progesterone USP: Dehydroepiandrosterone Micronized (DHEA): Testosterone Trit ) 2.5 : 25 : 2.5 : 0.1MG TROCHE, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

Affected lot / code info
Lot # 12312014:91@6, Exp 3/31/2015

Why it was recalled

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

Recalling firm

Firm
the Compounder
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
340 Marshall Ave Unit 100, N/A, Aurora, Illinois 60506-5649

Distribution

Quantity
60 troches
Distribution pattern
Nationwide

Timeline

Recall initiated
2015-03-10
FDA classified
2015-11-10
Posted by FDA
2015-11-18
Terminated
2016-05-19
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0183-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.