FDA Drug Recalls

Recalls / Class II

Class IID-0226-2016

Product

TRIEST 70/20/10 ( Estriol USP / Estradiol USP (E2) / Estrone (E1) Triturate) [909] 12.5MG/ML transdermal cream, dispensed in 1 mL prefilled amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

Affected lot / code info
Lot # 12222014:81@25, Exp 6/20/2015

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
24 (1mL) syringes
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-0226-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.