Arrow recalls large-bore CVC kits that may lack critical sticker with lot number, expiration date, and UDI. This affects medical use where missing info could impact safety.
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 large-bore multi-lumen central venous catheter kits that might not have a sticker with lot number, expiration date, or unique device ID. This is important because medical staff need this info for safe use and tracking.
Missing stickers prevent healthcare teams from verifying the product's expiration date and unique identification. This could lead to using expired or mislabeled equipment, potentially causing errors in patient treatment.
Healthcare professionals using these kits for short-term central venous access, especially those in settings where precise tracking is critical. Patients receiving treatments like chemotherapy or contrast media are at risk if the kit lacks proper identification.
Check for a sticker with lot number, expiration date, and Unique Device Identification (UDI) on the kit. The product code is CDA-22123-1A and the specific serial number is 13F17F0744.
Look for a sticker with lot number, expiration date, and Unique Device Identification (UDI) information on the kit.
The recall is because some kits may be missing a critical sticker with lot number, expiration date, and UDI information needed for safe medical use.
Check for the sticker with lot number, expiration date, and UDI information. If missing, contact Arrow for guidance.
The official recall notice does not specify a deadline for action.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1001-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1001-2018 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.
