Arrow recalls pressure injectable multi-lumen central venous catheter kits that may lack a sticker with lot number, expiration date, and UDI information. This affects medical use for short-term IV access.
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 pressure injectable multi-lumen central venous catheter kits that may be missing a sticker with lot number, expiration date, and UDI information. This could prevent proper tracking of the device and potentially lead to safety issues during medical use.
Missing lot numbers and expiration dates could make it difficult to track the device's safety and compliance. This might lead to improper use or failure to follow medical protocols during critical treatments.
Healthcare providers using the Arrow CVC kits for short-term IV access in medical settings. Patients receiving treatments like chemotherapy or contrast media may be at risk if the kit lacks proper identification.
Check for a sticker with lot number, expiration date, and Unique Device Identification (UDI) information on the kit. The product is used for short-term IV access in medical settings.
Look for a sticker containing the lot number, expiration date, and UDI information on the kit.
The recall is for kits that may be missing a sticker with lot number, expiration date, and UDI information, which could affect tracking and safety during medical use.
Check for the sticker with lot number, expiration date, and UDI information. If missing, contact Arrow for guidance.
The hazard is low risk as it involves missing identification information, not immediate safety risks like injury or malfunction.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0997-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0997-2018 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.
