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Class II: temporary or reversible health riskOngoing

Neogen Liceout Recall

LICEOUT, Liquid Lice Treatment for Human Use, Contents: 1 FL

Neogen Corporation · Lexington, KY

Risk level
Class II
Reported by FDA
Dec 4, 2024
Recall ID
D-0073-2025
Check your lot numberHow we source this data

Summary

Neogen recalled Liceout starting Oct 8, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0073-2025 on Dec 4, 2024. Reason: CGMP violations. Status: Ongoing.

Why it was recalled

CGMP violations.

Product description

LICEOUT, Liquid Lice Treatment for Human Use, Contents: 1 FL. OZ. (29.6 mL) per sachet, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53427-124-01

Lot numbers, UPCs & expiration codes

Lot LO09530; Exp 9/5/2025

Where it was sold

Product sold directly to one distributor consignee, Bob Barker Company, an American company that sells supplies to prisons, jails, and other institutions.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0073-2025
Classification
Class II
Status
Ongoing
Recall initiated
Oct 8, 2024
FDA report date
Dec 4, 2024
Quantity
5,328 sachets
Recall type
Voluntary: Firm initiated
Recalling firm
Neogen Corporation

Original FDA data

Every field from FDA enforcement report D-0073-2025, exactly as published.

Show all FDA fields
City
Lexington
State
KY
Status
Ongoing
Country
United States
Event ID
95823
Address
1847 Mercer Rd Ste A
Code information
Lot LO09530; Exp 9/5/2025
Postal code
40511-1001
Report date
Dec 4, 2024
Product type
Drugs
Recall number
D-0073-2025
Classification
Class II
Recalling firm
Neogen Corporation
Product quantity
5,328 sachets
Reason for recall
CGMP violations.
Voluntary / mandated
Voluntary: Firm initiated
Product description
LICEOUT, Liquid Lice Treatment for Human Use, Contents: 1 FL. OZ. (29.6 mL) per sachet, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53427-124-01
Distribution pattern
Product sold directly to one distributor consignee, Bob Barker Company, an American company that sells supplies to prisons, jails, and other institutions.
Recall initiation date
Oct 8, 2024
Initial firm notification
Letter
Center classification date
Nov 27, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0073-2025, published Dec 4, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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