Estradiol 22 mg pellet 99 recalled over manufacturing violations
- Recall date
- April 19, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Qualgen recalls Estradiol 22 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Of…
- Recall number
- D-0890-2017
- FDA classification
- Class II
- Brand / firm
- Qualgen
- Sold / distributed
- Nationwide.
Why it was recalled
CGMP deviations- Lack of Quality Assurance
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Estradiol 22 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 69761-022-01
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