Skip to content

MAHURKAR 8888135167Recalls & reported problems

Mozarc Medical US LLC · Acute Dual Lumen Catheter Tray High Flow Straight Extensions with IC Components · Class 2

All models of MAHURKAR (81)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521057333), received between Jul 21, 2020 and Jul 21, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (1 report).

10 other recalls cover devices cleared under the same FDA submission (K030209, K192302); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Migration or Expulsion of Device1
  • Product Quality Problem1

Patient problems

  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 21, 2020Migration or Expulsion of Device; Product Quality Problem; Migration or Expulsion of Device; Product Quality Problem

    ACCORDING TO THE REPORTER, DURING CHEST COMPRESSIONS, THE CATHETER SECUREMENT DEVICE (SUTURE WING) BROKE AND THE CATHETER DISLODGED FROM THE PATIENT. IT WAS ALSO STATED THAT THERE WAS A LEAK FROM THE CATHETERS EXIT SITE. CATHETER WAS NOT REPAIRED. THERE WAS NO REPORTED PATIENT OUTCOME.

    Patient problems: No Information

    MAUDE report 10302396 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K030209, K192302. One submission often covers many models, so check the product and lot details in each record.

  • Z-0421-2026 · Oct 17, 2025 · Open, Classified
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 13 cm;
  • Z-0422-2026 · Oct 17, 2025 · Open, Classified
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 16 cm;
  • Z-0425-2026 · Oct 17, 2025 · Open, Classified
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;
  • Z-0424-2026 · Oct 17, 2025 · Open, Classified
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
  • Z-0426-2026 · Oct 17, 2025 · Open, Classified
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Safety Components: 12 Fr/Ch (4.0 mm) x 24 cm;
  • Z-0423-2026 · Oct 17, 2025 · Open, Classified
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
  • Z-0877-2023 · Dec 7, 2022 · Open, Classified
    MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5cm, Straight Extensions, Kit - Model No. 8888135131; 13.5 cm, Curved Extensions,
  • Z-1955-2019 · Apr 29, 2019 · Terminated
    MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 8813793013 8813794005 8813794009 8813816005 8813816009 8813817005 8813817009 8815668007 88156
  • Z-0233-04 · Dec 2, 2003 · Terminated
    Mahurkar QPlus Dual Lumen Catheter Kit with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis, apheresis, and infusion. Reference: 8888-135192
  • Z-0234-04 · Dec 2, 2003 · Terminated
    Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis, apheresis, and infusion Reference: 8888-135195

Other CATHETER, HEMODIALYSIS, NON-IMPLANTED devices

All CATHETER, HEMODIALYSIS, NON-IMPLANTED devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page