Medline recalls 17 surgical tray kits with excess material on catheter hubs that could cause disconnection during arterial line procedures. Affected kits include ART1185B, ART255, ART350, ART355, ART475, ART535A, ART545A, ART775C, ART840, and ART890B from specific lot numbers.
The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
Medline is recalling 17 different surgical tray kits that contain catheters with excess material on the hub. This could cause the catheter to disconnect during use, potentially leading to complications in arterial line procedures.
The catheter hub has excess material that could cause the catheter to disconnect during use. This might lead to complications in arterial line procedures, such as bleeding or loss of blood flow.
Healthcare professionals using Medline's surgical tray kits for arterial line procedures are most at risk. Patients receiving these procedures may be affected if the catheter disconnects.
Check for the item numbers ART1185B, ART255, ART350, ART355, ART475, ART535A, ART545A, ART775C, ART840, or ART890B. The lot numbers listed in the recall include 2024082690 through 2024102890.
Look for the specific item numbers listed in the recall: ART1185B, ART255, ART350, ART355, ART475, ART535A, ART545A, ART775C, ART840, or ART890B.
Confirm the lot numbers are within the range 2024082690 to 2024102890 as listed in the recall.
The catheter hub has excess material that could cause the catheter to disconnect during use, potentially leading to complications in arterial line procedures.
The affected item numbers are ART1185B, ART255, ART350, ART355, ART475, ART535A, ART545A, ART775C, ART840, and ART890B.
Check the item number and lot number on your kit. If it matches the affected item numbers and lot numbers listed in the recall (2024082690 through 2024102890), it is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0991-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0991-2025 from Medline. 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.
