LICEOUT recalled over manufacturing violations
- Recall date
- October 8, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Neogen Corporation recalls LICEOUT, Liquid Lice Treatment for Human Use, Contents: 128 FL OZ. (3785.4 mL mL) per jug, Distributed By: Bob Barker C…
- Recall number
- D-0074-2025
- FDA classification
- Class II
- Brand / firm
- Neogen Corporation
- Sold / distributed
- Product sold directly to one distributor consignee, Bob Barker Company, an American company that sells supplies to prisons, jails, and other institutions.
Why it was recalled
CGMP violations.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
LICEOUT, Liquid Lice Treatment for Human Use, Contents: 128 FL OZ. (3785.4 mL mL) per jug, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53247-124-02
Get recall alerts
Free email alert whenever Neogen Corporation has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Neogen Corporation