MedComp recalls catheter repair kit AAC52001 with UDI 884908001891 due to potential connection failures causing blood loss or air emboli. Affected units include 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 its catheter repair kit (model AAC52001) because faulty connections could cause blood loss or air emboli. This is serious for patients using dialysis equipment.
The repair kit's female two-part luer connector can fail when attached to hemodialysis tubing, potentially causing blood loss or air emboli. This happens because the connection may not stay secure during use.
Patients using dialysis equipment with the recalled repair kit are most at risk. Healthcare providers who use this kit for catheter repairs may also be affected.
Check for the model AAC52001 with UDI 884908001891. Affected units have specific lot numbers: MCFW420, MCDD880, MCDN790, MCCK830, MCCV200, MCCX830, MCDB100, MCDT910, and MCFL210.
Identify the lot number on the repair kit packaging to see if it matches the affected lots listed: MCFW420, MCDD880, MCDN790, MCCK830, MCCV200, MCCX830, MCDB100, MCDT910, or MCFL210.
If you have the recalled kit, contact your healthcare provider for guidance on safe alternatives or repairs.
The recalled model is AAC52001 with UDI 884908001891.
Affected lot numbers are MCFW420, MCDD880, MCDN790, MCCK830, MCCV200, MCCX830, MCDB100, MCDT910, and MCFL210.
The recall does not specify a fix; affected users should contact their healthcare provider for alternatives.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-1118-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-1118-2018 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.
