FDA Drug Recalls

Recalls / Class II

Class IID-1471-2019

Product

Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection, packaged in a) 7.2 mL. b) 9.6 mL, c) 10.8mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.

Affected lot / code info
Lot #: a) 05032019@18, Exp. 08/04/2019; b) 05062019@20, Exp. 08/06/2019; c) 05132019@1, Exp. 08/13/2019.

Why it was recalled

Lack of Assurance of Sterility.

Recalling firm

Firm
First Pharma Associates LLC dba Riverpoint Pharmacy
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
1802 N Monroe St, Spokane, Washington 99205-4528

Distribution

Quantity
a) 14.4 mL, b) 9.6 mL, c) 10.8 mL
Distribution pattern
ID, WA only

Timeline

Recall initiated
2019-06-26
FDA classified
2019-07-11
Posted by FDA
2019-07-17
Terminated
2023-06-06
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1471-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls