MedComp recalls 12F X 60CM TESIO Catheter Sets with Y Adapter (REF CMD757) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
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 60CM TESIO catheter sets with Y adapters (REF CMD757) because faulty connections might cause blood loss or air emboli. This is serious for patients using hemodialysis tubing.
The female two-part luer connector can fail when connecting to hemodialysis blood tubing, leading to blood loss or air emboli. This happens because the connection isn't secure enough for medical use.
Patients using hemodialysis treatments with this catheter set are most at risk. The recall affects specific lot numbers and units sold with the UDI 884908005554.
Check for the product name: 12F X 60CM TESIO Catheter Set with Y Adapter (REF CMD757). Look for lot numbers MCCD870, MCDK730, MCDN640, MCCS670, MCDR570, or MCDS970. The unique device identifier (UDI) is 884908005554.
Look for signs of loose connections or leaks in the catheter set when attached to hemodialysis tubing.
The recall is due to potential connection failures that could cause blood loss or air emboli when used with hemodialysis blood tubing.
Check the lot numbers and UDI to confirm if your unit is affected. If it is, contact MedComp for the repair kit.
Yes, connection failures could lead to blood loss or air emboli, which are serious medical risks 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-1121-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-1121-2018 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.
