Arrow recalls some CVC kits that may lack critical labeling for lot numbers and expiration dates, risking incorrect use in medical treatments.
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 CVC kits that might be missing labels with important information like expiration dates and lot numbers. This could lead to incorrect medical use if the kit isn't properly identified.
Missing labels could prevent healthcare providers from verifying expiration dates and lot numbers. This might lead to using expired or incorrect kits during medical procedures.
Healthcare providers using Arrow CVC kits for short-term medical treatments may be affected. Patients receiving these kits are at risk if the missing labels cause incorrect use.
Check for a sticker with the lot number, expiration date, and Unique Device Identification (UDI) on the kit. The affected kits include specific model numbers like CA-45854-P1A 13F17F0071.
Look for a sticker with the lot number, expiration date, and Unique Device Identification (UDI) information on the kit.
The recall is happening because some kits may be missing critical labels with lot numbers, expiration dates, and Unique Device Identification (UDI) information.
Check for the sticker with the lot number, expiration date, and UDI information. If missing, contact Arrow for guidance.
The recall does not indicate a risk of serious injury; the hazard is limited to potential incorrect use due to missing labels.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0999-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0999-2018 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.
