Arrow recalls Multi Lumen Central Venous Catheterization Kits with possible incorrect Springwire Guide (SWG) that could cause complications during medical procedures. Affected kits were sold between February and November 2018.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Arrow is recalling Multi Lumen Central Venous Catheterization Kits that may contain an incorrect Springwire Guide (SWG). This could lead to complications during medical procedures if the kit is used improperly. The recall affects kits with specific product codes and expiration dates.
The kits may contain the wrong Springwire Guide (SWG), which could cause improper placement of catheters. This might lead to complications like infection or bleeding during medical procedures. The risk is not immediate but depends on proper use.
Healthcare professionals who use these kits for central venous catheterization are most at risk. Patients receiving procedures using the recalled kits could also be affected.
Check for product code ASK-12703-HH2 on the kit packaging. The kits were sold between February and November 2018 with expiration dates up to November 2018. Lot number 23F17C0652 is also associated with this recall.
Review the product code and expiration date on the kit packaging to confirm if it matches the recalled items.
The recall indicates a potential risk of improper catheter placement, but the hazard level is low risk as the issue may not cause serious injury in normal use.
Check for product code ASK-12703-HH2 with expiration dates between February and November 2018 and lot number 23F17C0652.
The recall does not specify a remedy, so contact Arrow International for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0650-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0650-2018 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.
