Arrow recalls pressure injectable multi-lumen catheter kits that may lack a sticker with lot number, expiration date, and UDI information. This affects medical devices used for short-term central venous 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 certain pressure injectable catheter kits that might be missing a sticker with important identification details. This could make it hard for healthcare providers to track the device's expiration and safety information.
The missing sticker means the lot number, expiration date, and Unique Device Identification (UDI) information aren't visible. This makes it difficult to verify the device's safety and expiration before use, which is critical for medical treatments.
Healthcare providers using the Arrow CVC kits for short-term central venous access are most at risk. Patients receiving treatments like chemotherapy or contrast media through these kits could be affected if the identification is missing.
Check for the sticker with lot number, expiration date, and UDI information on the kit. The affected kits include specific model numbers like 13F16L0007, 13F16M0013, 13F17A0296, 13F17D0110, and 13F17F0319.
Look for a sticker containing the lot number, expiration date, and Unique Device Identification (UDI) information on the kit.
The recall is happening because some kits may be missing the sticker with lot number, expiration date, and UDI information, which is necessary for tracking the device's safety and expiration.
Check for the sticker with lot number, expiration date, and UDI information. If missing, contact Arrow for guidance.
Yes, the affected model numbers include 13F16L0007, 13F16M0013, 13F17A0296, 13F17D0110, and 13F17F0319.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0995-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0995-2018 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.
