Arrow recalls multi-lumen central venous catheter kits that may lack a sticker with lot number, expiration date, and UDI information. This could affect product traceability and safety.
Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
Arrow is recalling multi-lumen central venous catheterization kits that might be missing a sticker with important identification details. This could make it harder to track the product and ensure it's safe for medical use.
The kits may lack a sticker with the lot number, expiration date, and Unique Device Identification (UDI) information. This makes it difficult to trace the product and verify its safety and compliance with medical standards.
Healthcare professionals who use these catheter kits for short-term medical treatments may be affected. Patients receiving care with these kits could be at risk if the missing sticker prevents proper identification.
Check for a sticker with the lot number, expiration date, and UDI information on the kit. The kits are labeled with model numbers like ASK-12703-PRJ, 13F17B0279, 13F17D0112, and ASK-15703-PRJ.
Look for a sticker containing the lot number, expiration date, and Unique Device Identification (UDI) information on the kit.
The recall is because some kits may be missing a sticker with the lot number, expiration date, and UDI information, which is needed for traceability and safety.
Check for the sticker with the lot number, expiration date, and UDI information. If missing, contact Arrow for guidance.
This is a low-risk issue as it affects product traceability but does not pose an immediate safety hazard like injury or death.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0994-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0994-2018 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.
