FDA Drug Recalls

Recalls / Class II

Class IID-0457-2016

Product

Test Cyp/Test Prop 1:1 Injection 100mg/mL, 120mg/mL, 150mg/mL, 160mg/mL, 170mg/mL, 200mg/mL, 300mg/mL, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

Affected lot / code info
all lots

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Western Drug
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
105 W Main St, Springerville, Arizona 85938-7203

Distribution

Quantity
75 containers
Distribution pattern
Nationwide in US: Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah

Timeline

Recall initiated
2015-10-19
FDA classified
2015-12-01
Posted by FDA
2015-12-09
Terminated
2016-10-01
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0457-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.