MasterPharm LLC recalls Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale,…
- Recall date
- June 9, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1363-2020
- FDA classification
- Class I
- Brand / firm
- MasterPharm LLC
- Sold / distributed
- FL and MD
Why it was recalled
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale, Store at room temperature, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
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