Testosterone 200 mg/Anastrozole 20 mg pellet recalled over sterility concerns
- Recall date
- October 17, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Qualgen, LLC recalls Testosterone 200 mg/Anastrozole 20 mg pellet, 1 count (NDC 69761-222-01), 6 count (NDC 69761-222-06), 12 count (NDC 697…
- Recall number
- D-0238-2019
- FDA classification
- Class II
- Brand / firm
- Qualgen, LLC
- Sold / distributed
- Nationwide.
Why it was recalled
Lack of Assurance of Sterility
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Testosterone 200 mg/Anastrozole 20 mg pellet, 1 count (NDC 69761-222-01), 6 count (NDC 69761-222-06), 12 count (NDC 69761-222-12), and 30 count (NDC 69761-222-30) vials, Rx Only, Qualgen, Edmond, OK 73013
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