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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

CarePoint Vet Syringes Recalled for Potential Green Substance on Plunger

Agency Publication Date: December 13, 2022
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Summary

Allison Medical, Inc. is recalling approximately 1,800 boxes of CarePoint Vet 60 mL syringes without needles because a green substance may be present on the plunger. While testing has shown the substance to be nontoxic, its potential effect on drug potency or chemical interactions is currently unknown. These veterinary syringes were distributed in Iowa and no injuries or incidents have been reported to date.

Risk

The presence of an unknown substance on the plunger could potentially interact with or degrade the medication being administered to an animal. This poses a risk to animal health through altered drug effectiveness or unknown chemical reactions.

What You Should Do

  1. Check your supply for CarePoint Vet 60 mL Syringes Without Needle with REF number 11-8360 and Lot number 80929.
  2. If you have animal health concerns, contact your veterinarian. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer or supplier for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: If you have animal health concerns, contact your veterinarian. Return any unused product to the place of purchase for a refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: CarePoint Vet 60 mL Syringe Without Needleby CarePoint Vet
Variants: 60 mL
Model:
11-8360
Lot Numbers:
80929

REF/Lot: 11-8360/ 80929

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91313
Status: Resolved
Manufacturer: Allison Medical, Inc.
Sold By: Authorized distributors
Manufactured In: United States
Units Affected: 1800 Boxes
Distributed To: Iowa
Agency Last Updated: December 21, 2022

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