Arrow recalls AGB+ Multi Lumen Central Venous Catheterization Kits with incorrect Springwire Guide (SWG) that could cause complications during medical procedures. Affected kits have specific product codes and expiration dates.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Arrow is recalling certain AGB+ Multi Lumen Central Venous Catheterization Kits because they may contain the wrong Springwire Guide (SWG). This could lead to complications during medical procedures. The recall affects kits with specific product codes and expiration dates.
The kits may contain an incorrect Springwire Guide (SWG) that could cause complications during medical procedures. This issue arises because the wrong SWG might not function properly, potentially leading to issues with catheter placement or patient safety.
Healthcare professionals using these kits for central venous catheterization are most at risk. Patients receiving procedures with the recalled kits could be affected.
Check for product codes CDC-42703-XP1A or CDC-47702-XP1A with expiration dates between February 2018 and November 2018. Lot numbers 23F16M0507 for CDC-42703-XP1A and 23F17A0533 for CDC-47702-XP1A are also affected.
Verify the product codes on the kit: CDC-42703-XP1A or CDC-47702-XP1A.
Ensure the kit's expiration date falls between February 2018 and November 2018.
Check for lot numbers 23F16M0507 (CDC-42703-XP1A) or 23F17A0533 (CDC-47702-XP1A).
The kits may contain the incorrect Springwire Guide (SWG) that could cause complications during medical procedures.
Check for product codes CDC-42703-XP1A or CDC-47702-XP1A with expiration dates between February 2018 and November 2018. Lot numbers 23F16M0507 for CDC-42703-XP1A and 23F17A0533 for CDC-47702-XP1A are also affected.
The recall does not require immediate discontinuation; healthcare professionals should check the product details to confirm if their kit is affected.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0655-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0655-2018 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.
