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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 Vet
Pets & Animals/Pet Medications

Ceva Animal Health, LLC: Hyliderm + PS and PhytoVet EFA Mousse Recalled for Fungal Contamination

Agency Publication Date: August 14, 2017
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Summary

Approximately 1,334 bottles of Hyliderm + PS Mousse and PhytoVet EFA Mousse pet skin treatments are being recalled due to the discovery of microbial contamination. Testing found the presence of Penicillium citrinum and Penicillium mallochii fungi in specific batches of these 6.8 FL OZ (200 mL) topical foam products. Consumers who have purchased these products for their pets should check the lot numbers and expiration dates on the packaging. To ensure the safety of your animals, you are advised to contact your veterinarian or pharmacist and return any unused product for a refund.

Risk

The products are contaminated with Penicillium citrinum and Penicillium mallochii fungi. Applying contaminated topical mousse to a pet's skin could cause or worsen skin infections, particularly in animals with existing skin conditions or weakened immune systems.

What You Should Do

  1. Check your product packaging for the following identifying details: Hyliderm + PS Mousse (6.8 FL OZ) with NDC 13744-127-01 and Lot 160301B (Exp 4/11/2018) or Lot 170321B (Exp 3/18/2019).
  2. Check your product packaging for Henry Schein PhytoVet EFA Mousse (6.8 FL OZ) with NDC 11695-7200-1 and Lot 160301A (Exp 4/11/2018) or Lot 170321A (Exp 3/18/2019).
  3. Immediately stop using the affected mousse on your pet if your bottle matches the lot numbers and expiration dates listed above.
  4. Contact your veterinarian or pharmacist for guidance regarding your pet's health and to discuss alternative skin treatments.
  5. Return any unused or opened bottles of the recalled product to the place of purchase or the pharmacy where it was obtained for a full refund.
  6. Contact Ceva Animal Health, LLC for further instructions or to report any adverse health events at their Lenexa, Kansas headquarters.
  7. For additional questions, contact the FDA's Center for Veterinary Medicine at 1-240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Veterinary drug refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Hyliderm + PS Mousse, Phytosphingosine salicyloyl 0.05% (6.8 FL OZ)
Model:
NDC: 13744-127-01
V-0279-2017
FSHYLPS3068
FSHYLPS3068CL
Lot Numbers:
160301B (Exp Date 4/11/2018)
170321B (Exp Date 3/18/2019)
Date Ranges: April 11, 2018, March 18, 2019
Product: Henry Schein, PhytoVet EFA Mousse, Phytosphingosine 0.05% (6.8 FL OZ)
Model:
NDC: 11695-7200-1
V-0280-2017
FSHYLPS3068HS
Lot Numbers:
160301A (Exp Date 4/11/2018)
170321A (Exp Date 3/18/2019)
Date Ranges: April 11, 2018, March 18, 2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 77386
Status: Resolved
Manufacturer: Ceva Animal Health, LLC
Sold By: Henry Schein; Sogeval Laboratories, Inc.; Veterinary clinics; Pet pharmacies
Manufactured In: United States
Units Affected: 2 products (764 bottles; 570 bottles)
Distributed To: Alabama, California, Colorado, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Maine, Michigan, Missouri, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Virginia, Washington

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