Arrow recalls Multi Lumen CVC Kits (Product Code CDC-15703-1A) due to potential incorrect Springwire Guide. Affected units expired Feb 2018 to Nov 2018. Contact for remedy.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Arrow is recalling Multi Lumen CVC Kits that may contain an incorrect Springwire Guide. This could lead to improper catheter placement and complications during medical procedures.
The incorrect Springwire Guide could cause improper catheter placement. This might lead to complications such as infection or damage to blood vessels during medical procedures.
Healthcare professionals using these kits for central venous catheter procedures are most at risk. Patients receiving these kits may experience complications if the catheter is misplaced.
Check for Product Code CDC-15703-1A on the kit. These kits were sold between February 2018 and November 2018.
Look for Product Code CDC-15703-1A and expiration dates between February 2018 and November 2018.
Product Code CDC-15703-1A.
These kits were sold between February 2018 and November 2018.
The recall record does not specify a remedy.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0654-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0654-2018 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.
