Cardinal Health recalls Monoject 201 Vet Pak hypodermic needles due to potential sterility compromise from manufacturing defects. Affected items have item code 8881201522 and lot number 905662.
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Cardinal Health is recalling Monoject 201 Vet Pak hypodermic needles because a manufacturing defect might compromise the sterility barrier. This could lead to infections if the needles are used without proper sterility.
The manufacturing defect in the cartridge component could allow contamination to reach the needle's sterility barrier. This might lead to infections if the needle is used without proper sterility.
Vet owners and animal caregivers who use these needles for pet vaccinations or treatments. The risk is low for most users since the defect is unlikely to cause immediate harm.
Check for item code 8881201522 and lot number 905662 on the needle packaging. The product is a 19-gauge x 1-1/2 inch hypodermic needle for veterinary use.
Look for item code 8881201522 and lot number 905662 on the needle packaging.
The recall is for potential sterility compromise due to a manufacturing defect, but the risk of infection is low.
Check the item code and lot number on the packaging to see if it's affected. No specific action is required beyond checking.
Look for item code 8881201522 and lot number 905662 on the packaging. If you have these details, it's affected.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2045-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2045-2019 from Cardinal Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
