Arrow recalls pressure injectable multi-lumen catheter kits with possible incorrect springwire guide. Affected kits may have safety risks. Consumers should check product codes and contact Arrow for details.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Arrow is recalling pressure injectable multi-lumen central venous catheterization kits that may contain an incorrect springwire guide. This could lead to safety issues during medical procedures if the guide doesn't function properly.
The incorrect springwire guide may not function properly during catheter insertion, potentially causing injury or procedure failure. This could lead to complications like bleeding or infection if the catheter isn't placed correctly.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving care with these kits may also be affected if the incorrect guide causes complications.
Check for product code ASK-15703-PRWJ on the kit packaging. The kits were sold between February 2018 and November 2018 with lot number 13F17C0400.
Look for product code ASK-15703-PRWJ and lot number 13F17C0400 on the kit packaging.
This recall applies to specific pressure injectable multi-lumen catheter kits with product code ASK-15703-PRWJ sold between February 2018 and November 2018.
The recall record does not specify a replacement process or remedy.
The recall record does not specify a remedy, so contact Arrow directly 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-0651-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0651-2018 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.
