Arrow recalls two types of central venous access kits due to potential sterility issues. Certain lots may not be completely sealed, risking contamination during medical procedures. Affected products include specific product numbers and lot numbers.
Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
Arrow is recalling two types of central venous access kits that may not be completely sealed, which could lead to contamination during medical procedures. This recall affects specific product numbers and lot numbers sold to hospitals and clinics.
The kits may not seal properly, which can compromise sterility. If the kit is not sterile, it could introduce harmful bacteria during medical procedures, potentially causing infections.
Hospitals and clinics that use these kits for medical procedures are most at risk. Patients receiving procedures with these kits could face contamination risks.
Check for product numbers ASK-11242-PHP or CDC-11242-1A. Look for specific lot numbers listed: 13F17D0179, 13F17B0232, 13F17C0357, 13F17D0312, 13F17E0289, 13F17F0154, 13F17F0327, 13F17F0614.
Look for product numbers ASK-11242-PHP or CDC-11242-1A on the kit packaging.
Check if your kit has any of the listed lot numbers: 13F17D0179, 13F17B0232, 13F17C0357, 13F17D0312, 13F17E0289, 13F17F0154, 13F17F0327, 13F17F0614.
Certain lots of these kits may not be completely sealed, which could compromise sterility and lead to contamination during medical procedures.
Check the product number and lot number to see if it's affected. If it is, contact Arrow for further instructions.
If the kit is not sterile, it could introduce harmful bacteria during procedures, potentially causing infections. However, the recall is for specific lots and not all kits are affected.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1323-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1323-2018 from Arrow. 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.
