Drug & medication recalls Moderate risk

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

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