Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

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.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Vet
Medications & Supplements/Veterinary Medicines

Durotec Usa Company: Uddercare and Organic Wash Teat Wash Recalled for Bacterial Contamination

Agency Publication Date: February 12, 2008
Share:
Sign in to monitor this recall

Summary

Durotec Usa Company has recalled approximately 14,000 syringes of UDDERCARE Washing Liquid and Organic Wash because the products are contaminated with bacteria. These products are used as a teat wash for dairy cows and were distributed in 30 ml syringes packaged in cartons of 20. The recall specifically includes UDDERCARE syringes manufactured in June 2007 and sold to distributors in Washington, California, and Oregon. Consumers should immediately stop using these products and contact their veterinarian or the manufacturer for guidance on returns.

Risk

The teat wash is contaminated with bacteria, which can lead to infections in dairy cows and potentially compromise the safety or quality of the milk produced. While no specific injuries or animal illnesses were reported, bacterial contamination in veterinary products used on food-producing animals poses a moderate risk to animal health.

What You Should Do

  1. Check your dairy supply inventory for UDDERCARE Washing Liquid or Organic Wash in 30 ml syringes.
  2. Verify the identifying details: for UDDERCARE, look for Lot J161 with a manufacture date of 06/07 and an expiration date of 06/10.
  3. Immediately stop using the contaminated product to prevent the risk of bacterial infection in livestock.
  4. Contact Durotec Usa Company at 2600 Se 131st Ave, Vancouver, Washington, 98683-5422, or contact your specific distributor in Rochester, WA or Petaluma, CA for instructions on returning the product for a refund.
  5. Consult with a veterinarian if you have concerns about the health of dairy cows that were treated with these products.
  6. For additional information, contact the FDA Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

💰Full Refund

Veterinary product refund or replacement contact

How to: Contact your veterinarian or the manufacturer for guidance. Return any unused product to the place of purchase for a refund and contact the manufacturer for further instructions.

Affected Products

Product: UDDERCARE Washing Liquid (30 ml syringes)
Model:
Recall #: V-024-2008
Lot Numbers:
J161
Date Ranges: Manufacture date 06/07, Exp. 06/10
Product: Organic Wash (30 ml syringes)
Model:
Recall #: V-025-2008

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 45952
Status: Resolved
Manufacturer: Durotec Usa Company
Sold By: Rochester, WA Distributor; Petaluma, CA Dairy Supply; Distributors in Washington, Oregon, and California
Manufactured In: United States
Units Affected: 2 products (7000 tubes to distributors in California, Oregon and Washington; 7000 units of UDDERCARE to distributors in California, Oregon and Washington. Number of units of Oganic Wash not known.)
Distributed To: Washington, California, Oregon

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 · Raw API Response