FDA Enforcement Class II Terminated

Duo-Flow XTP Straight Full Set; Hemodialysis catheter insertion kits, AAC02106 AAC02107 AAC02108

Recall: Z-2932-2018 · Reported September 5, 2018

Enforcement

Recall Number
Z-2932-2018
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 XTP Straight Full Set; Hemodialysis catheter insertion kits, AAC02106 AAC02107 AAC02108

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

MCAW430, MCBR560, MCCX620 MCCF020 MCFK440 MKAY620

Distribution

Nationwide distribution; worldwide distribution.

Quantity

N/A