MedComp recalls TWO PART ADAPTER REF MCTLA2000 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 a two-part adapter (model MCTLA2000) that may cause blood loss or air emboli if connections fail. This is serious because medical devices are critical for patient safety.
The adapter can disconnect from hemodialysis tubing, leading to blood loss or air entering the bloodstream. This could cause serious complications during dialysis treatments.
Patients using hemodialysis equipment with this adapter are most at risk. Healthcare providers who use the adapter for blood tubing connections may also be affected.
Check for the model number MCTLA2000 on the adapter. Affected units have specific lot numbers: MCFF700, MCFB160, MKAG11O, MCDP590, MCDS140, or MCFSOSO. The unique device identifier (UDI) is 884908027310.
Immediately stop using the adapter if it is part of your hemodialysis equipment.
No, the adapter may cause connection failures leading to blood loss or air emboli, so it should not be used.
The model number is MCTLA2000.
Affected lot numbers are MCFF700, MCFB160, MKAG11O, MCDP590, MCDS140, and MCFSOSO.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-1125-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-1125-2018 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.
