MedComp recalls Duo-Flow IJ Full Tray models with potential suture wing cracks causing catheter dislocation, bleeding, or air emboli. Six complaints reported without serious injury.
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 IJ Full Tray medical devices because suture wings might crack or break. This could lead to catheter dislocation, bleeding, or air emboli in patients. The recall has six reported complaints with no serious injuries or deaths.
Suture wings in the Duo-Flow IJ Full Tray can crack or break during use. This may cause catheter dislocation, bleeding, or air emboli in patients. The firm has received six complaints about broken suture wings without serious injuries or deaths.
Patients using Duo-Flow IJ Full Trays for medical procedures may be affected. Healthcare providers and patients using the specific models are most at risk.
Check for models listed in the product names: MCDLT114IJ, MCDLT116IJ, MCDLT118IJ, and others ending with specific codes like MCBA810 or MCBH13D. The devices were sold by MedComp for medical use.
Identify your Duo-Flow IJ Full Tray model by checking the product codes listed in the recall notice.
The recall reports six complaints of broken suture wings without serious injuries or deaths, so the risk is low.
Check if your device has a model code from the list: MCDLT114IJ, MCDLT116IJ, MCDLT118IJ, or other codes like MCBA810 or MCBH13D.
The recall does not specify a remedy, so contact MedComp directly for guidance.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-2935-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-2935-2018 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.
