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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

Washington Homeopathic Products, Inc.: Homeopathic Pet Medications Recalled for Manufacturing Quality Deviations

Agency Publication Date: December 13, 2019
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Summary

Washington Homeopathic Products, Inc. is recalling approximately 183,984 bottles of various HomeoPet and EquioPathics veterinary medications including WRM Clear and Host No More formulas for dogs, cats, and horses. These products were not manufactured under Current Good Manufacturing Practices (CGMP), which means the company cannot guarantee their safety, quality, or purity. Consumers who have these pet medications should contact their veterinarian or pharmacist for guidance and return any unused product to the place of purchase for a full refund.

Risk

Failure to follow good manufacturing practices can lead to products that are contaminated, contain incorrect ingredient levels, or are otherwise unsafe for animal use. Because these products did not meet required quality standards during production, they may pose a health risk to pets through unpredictable side effects or lack of efficacy.

What You Should Do

  1. Check your pet medication bottles for the following product names: HomeoPet K9 WRM Clear, HomeoPet K9 Host No More, HomeoPet Feline WRM Clear, HomeoPet Feline Host No More, or HomeoPet EquioPathics Wrm Clear.
  2. Verify the lot numbers on your packaging against the affected list: for K9 WRM Clear (Lots 27510, 27943, 28236, 28867, 28903, 29275, 29291, 29473, 29627, 29635, 29689); for K9 Host No More (Lots 27943, 29029, 29689, 27510, 27511); for Feline WRM Clear (Lots 27499, 27511, 27579, 28383, 28867, 28903, 29022, 29029, 29152, 29275, 29409, 29590, 29627, 29635); for Feline Host No More (Lots 28236, 29590); and for EquioPathics Wrm Clear (Lots 28565, 29353).
  3. Stop using the affected pet medications immediately to prevent potential health risks to your animals.
  4. Contact your veterinarian or a pharmacist for guidance regarding your pet's health and to discuss alternative treatments.
  5. Return any unused portion of the recalled product to the place of purchase for a full refund and contact Washington Homeopathic Products, Inc. at their Berkeley Springs, WV location for further instructions.
  6. For additional questions, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

๐Ÿ’ฐFull Refund

Full refund upon return.

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

Affected Products

Product: HomeoPet K9 WRM Clear
Model:
V-0331-2020
Lot Numbers:
27510
27943
28236
28867
28903
29275
29291
29473
29627
29635
29689
Product: HomeoPet K9 Host No More
Model:
V-0332-2020
Lot Numbers:
27943
29029
29689
27510
27511
Product: HomeoPet Feline WRM Clear
Model:
V-0333-2020
Lot Numbers:
27499
27511
27579
28383
28867
28903
29022
29029
29152
29275
29409
29590
29627
29635
Product: HomeoPet Feline Host No More
Model:
V-0334-2020
Lot Numbers:
28236
29590
Product: HomeoPet EquioPathics Wrm Clear
Model:
V-0335-2020
Lot Numbers:
28565
29353

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84354
Status: Resolved
Manufacturer: Washington Homeopathic Products, Inc.
Sold By: HomeoPet
Manufactured In: United States
Units Affected: 5 products (58,397 bottles; 20,849 bottles; 91,509 bottles; 10,698 bottles; 2531 bottles)
Distributed To: Nationwide
Agency Last Updated: December 19, 2019

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