FDA Drug Recalls

Recalls / Class II

Class IID-0895-2017

Product

Estradiol 10 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only , For Subcutaneous Use Only Rx Only Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-010-01

Affected lot / code info
Lot# C021; Exp. 08/20/17 Lot# B160, Exp. 12/29/17 Lot# B140; Exp. 11/15/17 Lot# B107; Exp. 09/29/17 Lot# B079; Exp. 08/15/17 Lot# B046; Exp. 06/01/17

Why it was recalled

CGMP deviations- Lack of Quality Assurance

Recalling firm

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

Distribution

Quantity
5,260 pellets.
Distribution pattern
Nationwide.

Timeline

Recall initiated
2017-04-19
FDA classified
2017-06-07
Posted by FDA
2017-06-14
Terminated
2021-09-24
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0895-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.