FDA Drug Recalls

Recalls / Class II

Class IID-0230-2019

Product

Estradiol 6 mg pellet, 1 count (NDC 69761-006-01), 6 count (NDC 69761-006-06), 12 count (NDC 69761-006-12), and 30 count (NDC 69761-006-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013

Affected lot / code info
Lots: D007 BUD: 01/09/2019; D060 BUD: 3/14/2019

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-0230-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.