Arrow recalls PICC kits with missing lot number stickers. This affects medical devices used for short-term central venous access. Check your kit for the required sticker to avoid potential safety issues.
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 PICC kits that may be missing a sticker with lot number, expiration date, and unique device identification. This could lead to improper use or safety risks if the kit isn't properly identified.
The missing sticker means the kit's lot number, expiration date, and unique device ID aren't visible. This could lead to improper use or safety risks if the kit isn't properly identified during medical procedures.
Healthcare providers using Arrow PICC kits for short-term central venous access are most at risk. Patients receiving these kits may be affected if the missing sticker causes identification issues.
Check for a sticker with the lot number, expiration date, and Unique Device Identification (UDI) on the kit. The affected kits have model numbers like 13F16J0286 or 13F17A0217.
Look for a sticker with the lot number, expiration date, and Unique Device Identification (UDI) on the kit.
The recall is happening because some kits may be missing the sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
Check the kit for the sticker with the lot number, expiration date, and UDI. If missing, contact Arrow for guidance.
The missing sticker could lead to improper use or safety risks if the kit isn't properly identified during medical procedures.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0996-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0996-2018 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.
