FDA Drug Recalls

Recalls / Class II

Class IID-0227-2016

Product

TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol USP (E3)) (23) 5MG capsules, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

Affected lot / code info
Lot # 12302014:78@17, Exp 12/30/2015, Lot # 03032015:04@4, Exp 3/2/2016

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
120 capsules
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-0227-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.