US Drug Recall Register
Class III · Low risk Terminated Initiated Jun 8, 2018 (8 years ago)

ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date.

What was recalled

ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01

Recalling firm
Qualgen, LLC
NDC code
69761-020-01
Origin
OK, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0892-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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