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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

LICEOUT Liquid Lice Treatment Recalled for Manufacturing Violations

Agency Publication Date: November 27, 2024
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Summary

Neogen Corporation is recalling 13,656 units of LICEOUT Liquid Lice Treatment, including 1 fl. oz. sachets and 128 fl. oz. jugs. This recall was issued due to Current Good Manufacturing Practice (CGMP) violations, which means the product was not manufactured according to required safety and quality standards. These products were distributed to prisons, jails, and other institutional facilities through the Bob Barker Company.

Risk

Because the product was manufactured in violation of standard safety protocols, its quality and effectiveness cannot be guaranteed. While no specific injuries have been reported, consumers or facility staff using the product should be aware that manufacturing failures can lead to unintended side effects or reduced efficacy.

What You Should Do

  1. This recall affects LICEOUT Liquid Lice Treatment for Human Use sold in 1 fl. oz. sachets (NDC 53427-124-01) and 128 fl. oz. jugs (NDC 53247-124-02) distributed by the Bob Barker Company.
  2. To identify the 1 fl. oz. sachets, check for lot number LO09530 with an expiration date of September 5, 2025.
  3. To identify the 128 fl. oz. jugs, check the packaging for the lot number and expiration date. See the Affected Products section below for the full list of affected codes.
  4. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: LICEOUT Liquid Lice Treatment (1 fl. oz.)
Variants: 1 FL. OZ. (29.6 mL) per sachet
Lot Numbers:
LO09530 (Exp 9/5/2025)
NDC:
53427-124-01

Distributed by Bob Barker Company, Inc.

Product: LICEOUT Liquid Lice Treatment (128 fl. oz.)
Variants: 128 FL. OZ. (3785.4 mL) per jug
Lot Numbers:
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)
NDC:
53247-124-02

Distributed by Bob Barker Company, Inc.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95823
Status: Active
Manufacturer: Neogen Corporation
Sold By: Bob Barker Company
Manufactured In: United States
Units Affected: 2 products (5,328 sachets; 8,328 jugs)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.