FDA Drug Recalls

Recalls / Class II

Class IID-0686-2017

Product

Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.

Affected lot / code info
Lot #s: 09018, Exp 04/17/17; 09023, Exp 04/22/17; 09024, Exp 04/23/17; 09027, Exp 04/25/17; 09031, Exp 04/30/17; 10005, Exp 05/06/17; 10010, Exp 05/09/17; 11022, Exp 06/10/17; 11038, Exp 06/18/17; 11044, Exp 07/04/17; 12003, Exp 07/08/17; 12010, Exp 07/12/17; 12021, Exp 07/30/17.

Why it was recalled

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Recalling firm

Firm
Isomeric Pharmacy Solution, LLC
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
2401 S Foothill Dr Ste D, N/A, Salt Lake City, Utah 84109-1479

Distribution

Quantity
2,156 vials
Distribution pattern
Nationwide in the USA and Puerto Rico

Timeline

Recall initiated
2017-04-06
FDA classified
2017-04-26
Posted by FDA
2017-05-03
Terminated
2017-08-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0686-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.