Medical Components, Inc dba MedComp: Medical Device Recall in 2018 - (Recall #: Z-2934-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set; DL11/24 . Hemodialysis catheter insertion kits

Product Classification:

Class II

Date Initiated: July 12, 2018

Date Posted: September 5, 2018

Recall Number: Z-2934-2018

Event ID: 80581

Reason for Recall:

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.

Status: Terminated

Product Quantity: N/A

Code Information:

MCAL840 MCBB800 MCBW450 MCCH690

Distribution Pattern:

Nationwide distribution; worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated