MedComp recalls repair kit RPK-01 with UDI 884908039856 due to potential blood loss or air emboli from connection failures in hemodialysis tubing.
There is the potential for connection failures related to the female two-part luer to hemodialysis blood tubing lines, etc. which may contribute to blood loss or air emboli.
MedComp is recalling its Repair Kit RPK-01 (UDI 884908039856) because faulty connections could cause blood loss or air emboli during hemodialysis treatments. This is serious for patients using dialysis equipment.
The repair kit's female two-part luer connector may fail to connect properly with hemodialysis blood tubing, leading to blood loss or air emboli. This can happen during normal use when replacing damaged parts.
Patients using hemodialysis machines with this repair kit are most at risk. The kit is used to replace damaged connectors in dialysis tubing systems.
Check for the repair kit with UDI 884908039856. Lot numbers include MCCC310, MCCA800, MCFH990, and others listed in the recall notice.
Identify the repair kit using the UDI 884908039856 or lot numbers listed in the recall.
The MedComp Repair Kit RPK-01 is used to replace damaged female connectors, clamps, or repair extensions in hemodialysis tubing systems.
Connection failures could cause blood loss or air emboli during hemodialysis treatments.
Look for the UDI 884908039856 or lot numbers like MCCC310, MCCA800, MCFH990, and others listed in the recall notice.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-1127-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-1127-2018 from MedComp. 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.