Cardinal Health recalls Monoject 201 Vet Pak Hypodermic Needles due to potential sterility barrier compromise from manufacturing defects. Affected items have item code 8881201654 and lot number 902108.
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 infection if the needle is used after the barrier is breached.
The manufacturing defect in the cartridge component could weaken the sterility barrier of the needle. If the barrier is compromised, the needle might become contaminated, increasing the risk of infection during animal injections.
Vet owners and pet owners who use the recalled Monoject 201 Vet Pak Hypodermic Needles for animal treatments. Those with the specific item code 8881201654 and lot number 902108 are most at risk.
Check for the item code 8881201654 and lot number 902108 on the needle packaging. The product is a 16-gauge hypodermic needle with a length of 1-1/2 inches.
Look for item code 8881201654 and lot number 902108 on the needle packaging.
The recall is for potential sterility barrier compromise, which could lead to infection if the needle is used after the barrier is breached. However, the risk is low and not immediately dangerous in normal use.
Check for item code 8881201654 and lot number 902108 on the needle packaging. The product is a 16-gauge hypodermic needle with a length of 1-1/2 inches.
The recall does not specify a remedy, so you should check the product details and contact Cardinal Health if you have concerns.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2047-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2047-2019 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.
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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.
