Arrow recalls certain multi-lumen central venous catheterization kits due to potential sterility issues from incomplete sealing. Affected kits include specific model numbers and lot numbers listed in the recall notice.
Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
Arrow has recalled certain multi-lumen central venous catheterization (CVC) kits because some may not be completely sealed, risking contamination. This could lead to infections if used in medical procedures. Patients and healthcare providers should check their kit details against the list provided.
The kits may not be fully sealed, which can compromise sterility during medical procedures. This risk could lead to infections if the catheters are used without proper sterility.
Healthcare providers and patients using the recalled CVC kits for medical procedures are most at risk. The specific kits and lot numbers listed in the recall affect those who have purchased or used the products.
Check the product name and part number on the kit. Affected kits include specific model numbers like AK-42703-P1A and lot numbers such as 13F17A0135. The recall lists 42 different model numbers and lot numbers.
Identify the product name and part number on the kit to see if it matches the recalled models listed in the notice.
The recall includes specific multi-lumen central venous catheterization kits with model numbers like AK-42703-P1A and lot numbers such as 13F17A0135. The full list is provided in the recall notice.
The recall does not require immediate discontinuation; however, you should check if your kit is affected before use.
The recall does not specify a remedy, so you should contact Arrow International for further instructions if your kit is affected.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1326-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1326-2018 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.
