Medical Components, Inc dba MedComp: Medical Device Recall in 2018 - (Recall #: Z-2933-2018)

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:

Double Lumen CRRT/ABP Catheter Set; Hemodialysis catheter insertion kits, DL 11/15 DL 11/20 DL 9/15

Product Classification:

Class II

Date Initiated: July 12, 2018

Date Posted: September 5, 2018

Recall Number: Z-2933-2018

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:

MCAJ510 MCAP860 MCAZ820 MCCB890 MCCJ250 MCDF160 MCDQ630 MCFF200 MCFF620 MCFK200 MCFV440 MKAK310 MCAW770 MCBW430 MCCH320 MCCJ690 MCFB450 MCFF930 MCFV450 MKAK320 MKAV210 MCAY080 MCBD600 MCBP740 MCBW440 MCCA030 MCCH330

Distribution Pattern:

Nationwide distribution; worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated