Arrow recalls Pressure Injectable Multi-Lumen CVC Kits due to missing critical safety checklists for central line insertions. This may lead to errors during medical procedures.
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
Arrow is recalling Pressure Injectable Multi-Lumen CVC Kits because they lack essential safety checklists for central line insertions. This could lead to medical errors if used without the required procedures.
The kits do not include the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist. These tools are meant to guide clinicians through best practices during central line insertions. Without them, errors in the procedure could occur.
Healthcare professionals using the kit for central line insertions are most at risk. Patients receiving these procedures may be affected if the checklists are missing.
The recalled kits have the model CDC-15703-P1A and part number 13F16J0336. They were sold by Arrow International Inc.
Ensure the kit includes the Central Venous Catheter Placement Procedures Note and Central Line Insertion Checklist.
The kit does not contain the Central Venous Cath: Placement Procedures Note or Central Line Insertion Checklist, which are tools to guide clinicians during central line insertions.
The recall record does not specify a remedy, so check if the kit includes the required checklists.
The missing checklists could lead to errors during central line insertions, but the recall indicates a low-risk situation.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1165-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1165-2018 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.
