MenoPower recalled over manufacturing violations
- Recall date
- October 9, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Sprayology recalls MenoPower, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-00…
- Recall number
- D-0109-2019
- FDA classification
- Class II
- Brand / firm
- Sprayology
- Sold / distributed
- Distributed Nationwide in the USA
Why it was recalled
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
MenoPower, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0014-1 and Tester NDC 61096-1014
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