Arrow recalls Arterial Line Kit with Sharps Safety Features (Product Code ASK-04018-OH1) due to unsealed packaging risking sterility compromise. Affected lot numbers include 13F17E0562, 13F17G0537, 13F17K0188, 13F17L0167.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Arterial Line Kits with Sharps Safety Features because unsealed packaging could compromise sterility. This means the kits might not be sterile when used, increasing infection risk during medical procedures.
The packaging may not seal properly, allowing contamination. If the kit isn't sterile when used, it could introduce infections during medical procedures.
Healthcare professionals using the Arterial Line Kit for medical procedures are most at risk. Patients receiving these kits could face infection if the product isn't sterile.
Check for the product code ASK-04018-OH1 on the kit. Affected lots include 13F17E0562, 13F17G0537, 13F17K0188, and 13F17L0167.
Look for the lot numbers 13F17E0562, 13F17G0537, 13F17K0188, or 13F17L0167 on the kit packaging.
The recall states unsealed packaging may compromise sterility, so affected kits should not be used until the issue is resolved.
Check the lot number on the kit. If it matches the affected numbers, stop using it and contact Arrow for instructions.
Look for the product code ASK-04018-OH1 and the specific lot numbers listed: 13F17E0562, 13F17G0537, 13F17K0188, 13F17L0167.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1969-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1969-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
