FDA Enforcement
Class II
Terminated
Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set; DL11/24 . Hemodialysis catheter insertion kits
Recall: Z-2934-2018
·
Reported September 5, 2018
Enforcement
- Recall Number
- Z-2934-2018
- Event ID
- 80581
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Medical Components, Inc dba MedComp
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- September 5, 2018
- Initiation Date
- July 12, 2018
- Classification Date
- August 25, 2018
- Termination Date
- July 2, 2020
- Address
- 1499 Delp Dr, N/A, Harleysville, PA, 19438-2936, United States
Description
Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set; DL11/24 . Hemodialysis catheter insertion kits
Reason
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.
Code Info
MCAL840 MCBB800 MCBW450 MCCH690
Distribution
Nationwide distribution; worldwide distribution.
Quantity
N/A