CLASS II ONGOING Drug recall · Reported 4 Dec 2024 · FDA Enforcement Report
Liceout, Liquid Lice Treatment for Human Use, Contents: mL) per jug recalled
Neogen is recalling Liceout, Liquid Lice Treatment for Human Use, Contents: mL) per jug. The recall was initiated on 8 Oct 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0074-2025
- FDA event ID
- 95823
- Recalling firm
- Neogen, Lexington, KY
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 8 Oct 2024
- FDA classified
- 27 Nov 2024
- Reported
- 4 Dec 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 8 Oct 2024 | Recall initiated by company | |
| 27 Nov 2024 | Classified by FDA | +50 days |
| 4 Dec 2024 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP violations.
Product as listed by the FDA
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
Where it was distributed
Product sold directly to one distributor consignee, Bob Barker Company, an American company that sells supplies to prisons, jails, and other institutions.
Questions about this recall
Why was it recalled?
CGMP violations.
Which lots are affected?
Lot, expiry: LO09530, exp 11/3/2024; LO13412, exp 12/7/2024; LO10263, exp 1/26/2025; LO11303, exp 5/10/2025; LO12153, exp 8/3/2025; LO12483, exp 9/5/2025; LO13183, exp 11/14/2025; LO106024, exp 2/29/2026; LO108624, exp 3/26/2026; LO110224, exp 4/11/2026
Where was it sold?
Product sold directly to one distributor consignee, Bob Barker Company, an American company that sells supplies to prisons, jails, and other institutions.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 95823This product is part of a recall event; the main page for the event is Liceout, Liquid Lice Treatment for Human Use, Contents: per sachet recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Liceout, Liquid Lice Treatment for Human Use, Contents: per sachet recalled | Neogen | Manufacturing (CGMP) Deviations | KY |
More recalls from Neogen
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Liceout, Liquid Lice Treatment for Human Use, Contents: per sachet recalled | Neogen | Manufacturing (CGMP) Deviations | KY |