Arrow recalls specific CVC kits that may lack critical labeling for lot numbers and expiration dates, potentially causing 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 not have the required labels showing lot numbers, expiration dates, and unique identifiers. This could lead to incorrect medical use if the labels are missing.
Missing labels mean healthcare providers might not know the expiration date or lot number, which is critical for ensuring the kit is safe and effective for medical use. This could lead to incorrect treatments or complications if the kit is used beyond its safe period.
Healthcare professionals using the recalled CVC kits for short-term medical treatments may be affected. Patients receiving these kits are at risk if the missing labels cause incorrect usage.
Check for the labels with lot numbers, expiration dates, and Unique Device Identification (UDI) information on the kit. The specific model numbers listed include 13F16M0047 through 13F17H0407.
Look for the sticker with lot number, expiration date, and UDI information on the kit.
The recall is happening because some of the kits may be missing critical labels that include lot numbers, expiration dates, and UDI information.
Check the kit for the required labels. If the labels are missing, contact Arrow for guidance.
Yes, the affected model numbers include 13F16M0047 through 13F17H0407.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0998-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0998-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
