MedComp recalls SOFT-LINE DUO-FLOW double lumen catheter sets (T94C, T9: 150 characters
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 specific catheter sets because suture wings can crack or break, which may cause catheter dislocation, bleeding, or air embolism. The recall follows six complaints of broken suture wings without serious injuries or deaths.
The suture wings in these catheter sets can crack or break, potentially causing the catheter to dislocate, leading to bleeding or air embolism in the patient. This has occurred in six reported cases without serious injury or death.
Healthcare professionals and patients using the recalled catheter sets are most at risk if the suture wings crack or break during use.
Check for catheter sets labeled T94C, T94M, T96M, T98M with model numbers like MCDA290, MHLQ370, or MHMZ270. These were sold by MedComp starting in 2019.
Identify the model number on the catheter set, which may be listed in the product names or codes provided in the recall notice.
Reach out to MedComp directly for assistance with the recall process or to confirm if your catheter set is affected.
The recall report states six complaints of broken suture wings without serious injury or death.
Check for model numbers T94C, T94M, T96M, or T98M with codes like MCDA290, MHLQ370, or MHMZ270.
Contact MedComp directly to determine if your catheter set is affected and to get guidance on next steps.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-2940-2018 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-2940-2018 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.
