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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

ZOETIS SERVICES LLC: Veterinary IV Sets Recalled for Cracks and Leaking

Agency Publication Date: December 9, 2016
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Summary

Approximately 992,227 units of various Zoetis Veterinary IV Sets are being recalled because cracks can develop at the Y-site of the tubing, leading to leaks during fluid administration. The recall includes 12 different models of primary and piggyback IV sets used for animal care, all of which are individually plastic-wrapped and sterilized. These products were distributed nationwide in the United States and Guam between late 2016 and early 2017. If you have these IV sets in your veterinary inventory, you should stop using them and contact the manufacturer for further instructions.

Risk

Cracks at the Y-site connector can cause the IV set to leak, which may result in improper delivery of fluids or medications to an animal and potential loss of sterility in the fluid path.

What You Should Do

  1. Identify your IV sets by checking the product names and lot numbers on the individual plastic wrapping or the case label. Affected products include various 70, 78, 80, 100, 103, 105, and 106-inch Primary and Piggyback IV sets.
  2. Check for the following specific lot numbers: 95264KY, 96213KY, 96215KY, 96287KY, 97196KY, 97199KY, 97200KY, 97388KY, 97389KY, 97390KY, 97391KY, 98215KY, 98216KY, 99196KY, 99197KY, and 99395KY.
  3. Verify if the expiration dates on your packaging fall between October 2020 (2020-10) and February 2021 (2021-02).
  4. Immediately stop using any IV sets that match these lot numbers or expiration ranges to avoid fluid leakage during use.
  5. Contact your healthcare provider or Zoetis Services LLC at 10 Sylvan Way, Parsippany, NJ, or through their official website for instructions on returning the product and obtaining a potential refund or replacement.
  6. For additional questions regarding this veterinary device recall, contact the FDA Center for Veterinary Medicine (CVM) at 240-402-7002.

Your Remedy Options

๐Ÿ“‹Other Action

Veterinary medical device safety notification and instructions

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: PRIMARY PIGGYBACK IV SET, 106 INCH A (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY PIGGYBACK IV SET, 80 INCH A (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 78 INCH - VENTED A (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 78 INCH A (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 70 INCH, 60 DROPS/ML A (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 103 INCH B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 105 INCH B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY PIGGYBACK IV SET, 106 INCH B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY PIGGYBACK IV SET, 100 INCH B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 78 INCH - VENTED B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 78 INCH B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02
Product: PRIMARY IV SET, 70 INCH, 60 DROPS/ML B (50 units per case)
Model:
V-0036-2017
Lot Numbers:
95264KY
96213KY
96215KY
96287KY
97196KY
97199KY
97200KY
97388KY
97389KY
97390KY
97391KY
98215KY
98216KY
99196KY
99197KY
99395KY
Date Ranges: 2020-10 to 2021-02

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 75732
Status: Resolved
Manufacturer: ZOETIS SERVICES LLC
Sold By: Authorized veterinary distributors
Manufactured In: United States
Units Affected: 992,227 units
Distributed To: Nationwide

Were You Affected by This Recall?

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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