Cardinal Health recalls 15G 1.829mm x 3.8cm Monoject Blunt Cannula cartridges due to potential sterility compromise from manufacturing defects. Affected lots: 905659, 905660, 906343.
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Cardinal Health is recalling certain Monoject Blunt Cannula syringes because a manufacturing defect might compromise their sterility barrier. This could lead to infections if the product is used after the barrier is breached.
The syringes have a manufacturing defect that could compromise the sterility barrier. If the barrier is breached, the product might not be sterile, increasing infection risk during use.
Healthcare professionals and patients using the recalled syringes for injections. Those with the specific lot numbers are most at risk.
Check for the item code 8881202314 and lot numbers 905659, 905660, or 906343 on the syringe packaging.
Look for the item code 8881202314 and lot numbers 905659, 905660, or 906343 on the syringe packaging.
The recall is due to a manufacturing defect that could compromise the sterility barrier of the product.
The official recall notice does not specify a remedy or action for affected products.
Lot numbers 905659, 905660, and 906343 are 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-2048-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2048-2019 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.
