Arrow recalls multi-lumen central venous catheter kits with blue flextip due to unsealed packaging potentially compromising sterility. Affected kits may cause infections if used improperly.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling certain multi-lumen central venous catheter kits because the packaging might not be sealed properly. This could lead to infections if the kit is used without proper sterility.
The unsealed packaging means the catheter kit might not stay sterile when opened. If the kit is used without proper cleaning or handling, it could lead to infections during medical procedures.
Healthcare professionals using the recalled kits for central venous catheterization are most at risk. Patients receiving these procedures could face infection if the kits are used without proper sterility.
Check for product code ASK-42703-RV1 and lot numbers 13F17B0020 through 13F17L0455. These kits were sold with blue FlexTip catheters and sharps safety features.
Look for product code ASK-42703-RV1 on the kit packaging.
Confirm the kit has one of the listed lot numbers: 13F17B0020, 13F17B0269, 13F17C0303, 13F17F0317, 13F17H0062, 13F17J0386, 13F17K0583, or 13F17L0455.
The packaging may not be sealed properly, which could compromise sterility and lead to infections if used without proper cleaning.
Check for product code ASK-42703-RV1 and lot numbers 13F17B0020 through 13F17L0455.
No, but you should check the product code and lot numbers to confirm if it's affected. If it is, contact Arrow for guidance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1998-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1998-2018 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.
