FDA Drug Recalls

Recalls / Class II

Class IID-0234-2019

Product

Testosterone 25 mg pellet, 1 count (NDC: 69761-125-01) and 30 count vials (NDC: 69761-125-30), Rx Only Qualgen, LLC, Edmond, OK 73013

Affected lot / code info
Lots: C235 BUD: 11/10/2018; C241 BUD: 11/17/2018; C251 BUD: 12/8/2018; C265 BUD: 12/28/2018; D008 BUD: 1/9/2019; D018 BUD: 1/19/2019; D022 BUD: 1/25/2019; D032 BUD: 2/7/2019; D037 BUD: 2/13/2019; D057 BUD: 3/8/2019; D061 BUD: 3/14/2019; D069 BUD: 3/23/2019

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Qualgen, LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
14844 Bristol Park Blvd, Edmond, Oklahoma 73013-1891

Distribution

Distribution pattern
Nationwide.

Timeline

Recall initiated
2018-10-17
FDA classified
2018-11-07
Posted by FDA
2018-11-14
Terminated
2020-06-04
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0234-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.