MedComp recalls Duo-Flow XTP Straight Full Sets and hemodialysis catheter insertion kits (AAC02106-02108) due to potential suture wing cracks causing catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious injury or death.
MedComp is recalling Duo-Flow XTP Straight Full Sets and hemodialysis catheter insertion kits (model numbers AAC02106-02108) because suture wings might crack or break. This could lead to catheter dislocation, bleeding, or air emboli in patients. The recall follows six reported complaints with no serious injuries or deaths.
The suture wings in these kits can crack or break during use, which may cause the catheter to become dislocated. This could lead to bleeding or air emboli (air bubbles entering the bloodstream) in patients. The firm has received six complaints about broken suture wings but no serious injuries or deaths.
Patients using hemodialysis catheters with these specific kits are most at risk. The recall applies to the Duo-Flow XTP Straight Full Sets and insertion kits sold with model numbers AAC02106, AAC02107, and AAC02108.
Check for model numbers AAC02106, AAC02107, or AAC02108 on the Duo-Flow XTP Straight Full Sets and hemodialysis catheter insertion kits. These products were sold with specific serial numbers like MCAW430, MCBR560, MCCX620, MCCF020, MCFK440, and MKAY620.
Look for model numbers AAC02106, AAC02107, or AAC02108 on the Duo-Flow XTP Straight Full Sets and hemodialysis catheter insertion kits.
No serious injuries or deaths have been reported; six complaints were received about broken suture wings.
The recall does not specify a remedy, so check the product model numbers and contact MedComp for further instructions.
Look for model numbers AAC02106, AAC02107, or AAC02108 on the Duo-Flow XTP Straight Full Sets and hemodialysis catheter insertion kits.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-2932-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-2932-2018 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.
