Arrow recalls specific multi-lumen catheter kits due to unsealed packaging potentially compromising sterility. Affected lot numbers include 13F17E0547 through 13F17L0150.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling certain multi-lumen central venous catheterization kits because the packaging may not be sealed properly, risking contamination. This could lead to infections if the kit is used without proper sterility.
The unsealed packaging could allow contaminants to enter the kit, potentially causing infections during medical procedures. This risk is specific to the sterility of the catheter kit and not a general safety hazard.
Healthcare professionals using the ARROWg+ard Blue PLUS Multi-Lumen Central Venous Catheterization Kit with lot numbers 13F17E0547 through 13F17L0150 are most at risk. Patients receiving these kits during procedures could be affected if the sterility is compromised.
Check the lot numbers on the packaging: 13F17E0547, 13F17F0680, 13F17G0214, 13F17J0347, or 13F17L0150. The product is the ARROWg+ard Blue PLUS Multi-Lumen Central Venous Catheterization Kit.
Look for lot numbers 13F17E0547 through 13F17L0150 on the ARROWg+ard Blue PLUS Multi-Lumen Central Venous Catheterization Kit packaging.
The recall states that the packaging may not be sealed properly, which could compromise sterility. If you have the affected lot numbers, stop using the kit until you confirm it's safe.
The recall does not specify a remedy, so you should check with Arrow International Inc. for guidance on handling the product.
Check the lot numbers on the packaging: 13F17E0547, 13F17F0680, 13F17G0214, 13F17J0347, or 13F17L0150.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2000-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2000-2018 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.
