MedComp recalls 12F X 40CM TESIO Catheter Sets with Y-adapter (ref CMD755) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers.
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 12F X 40CM TESIO catheter sets with Y-adapters (model CMD755) because faulty connections could cause blood loss or air emboli. This is serious for patients using hemodialysis equipment.
The catheter set's female connectors may fail to properly connect to hemodialysis tubing, leading to blood leaks or air entering the bloodstream. This could cause serious complications during dialysis treatments.
Patients using hemodialysis equipment with this catheter set are most at risk. The recall affects specific lot numbers of the catheter set sold for medical use.
Check for the model number CMD755 on the catheter set. Affected units have lot numbers including MCBS820, MCBM670, MCDY280, MCDW670, MCFX650, MCFW520, MCCC910, MCCJ210, MCDF970, MCCV540, MCFJ340, MCFQ090, and MCFS610.
Identify if your catheter set has lot numbers listed in the recall: MCBS820, MCBM670, MCDY280, MCDW670, MCFX650, MCFW520, MCCC910, MCCJ210, MCDF970, MCCV540, MCFJ340, MCFQ090, or MCFS610.
If your catheter set is affected, contact MedComp to receive the repair kit for replacing damaged connectors or clamps.
The recall is due to potential connection failures in the female connectors that could cause blood loss or air emboli during hemodialysis treatments.
Check the lot number on your catheter set. If it matches the listed numbers, contact MedComp for the repair kit to fix damaged connectors or clamps.
Yes, connection failures could lead to blood loss or air emboli, which are serious complications during hemodialysis.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-1120-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-1120-2018 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.
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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.
