Arrow recalls Blue Plus Pressure Injectable Quad-Lumen CVC kits missing lot numbers or expiration dates. This affects medical devices used for short-term central venous access. Contact Arrow for details.
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 some Blue Plus Pressure Injectable Quad-Lumen CVC kits because they may be missing a sticker with lot numbers, expiration dates, and unique device identification. This could lead to improper use or safety issues if the device isn't properly tracked.
Missing lot numbers, expiration dates, and unique device identifiers could prevent proper tracking of the device. This might lead to using expired or incorrect devices, which could cause treatment errors or safety issues.
Healthcare providers using Arrow CVC kits for short-term central venous access are likely affected. Patients receiving treatments like chemotherapy or contrast media may be at risk if the kit is missing critical identification.
Check for a sticker with the lot number, expiration date, and Unique Device Identification (UDI) on the Arrow CVC kit. The product codes listed include CDA-45854-P1A, 13F17C0325, 13F17D0283, and 13F17F0748.
Look for a sticker with the lot number, expiration date, and Unique Device Identification (UDI) on the kit.
The recall is for kits that may be missing a sticker with lot numbers, expiration dates, and unique device identification.
Check for the sticker with lot number, expiration date, and UDI. If missing, contact Arrow for guidance.
Yes: CDA-45854-P1A, 13F17C0325, 13F17D0283, and 13F17F0748.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1005-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1005-2018 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.
