Cardinal Health recalls Monoject Blunt Cannula 20G x 1.5" due to potential sterility barrier compromise from manufacturing defect. Affected items have specific item code and lot number.
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Cardinal Health is recalling a specific type of medical needle because a manufacturing defect might compromise its sterile packaging. This could lead to infection risks if the needle is used without proper sterility.
The manufacturing defect in the cartridge component could allow the sterility barrier to be compromised. This means the needle might not be sterile when used, increasing infection risk during medical procedures.
Healthcare professionals and patients who use the recalled Monoject Blunt Cannula needles. Those most at risk are individuals receiving injections with this specific needle model.
Check for the item code 8881202363 and lot number 907734 on the needle packaging. The product is a 20G x 1-1/2" (0.902 mm x 3.8 cm) Monoject Blunt Cannula.
Look for item code 8881202363 and lot number 907734 on the needle packaging.
The recall states a potential sterility barrier compromise from a manufacturing defect, which could increase infection risk if the needle is not sterile. However, the remedy is not specified in the record.
Check for item code 8881202363 and lot number 907734 on the needle packaging. The product is a 20G x 1-1/2" (0.902 mm x 3.8 cm) Monoject Blunt Cannula.
The recall record does not specify a remedy, so no action is required beyond checking if you have the recalled item.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2051-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2051-2019 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.
