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SPLIT CATH® III ASPC36-3PCE.Recalls & reported problems

Medical Components, Inc. · 14F X 36CM PRE-CURVED SPLIT CATH® III CATHETER SET (CUFF 31CM FROM TIP) · Class 2 · Implant

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884908004113), received between May 3, 2022 and May 3, 2022 — classified as 1 death.

The most frequently reported specific device problem is “Disconnection” (1 report).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Disconnection1

Patient problems

  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

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

  • DeathMay 3, 2022Disconnection; Disconnection

    DURING TREATMENT, THE PATIENT WAS FOUND UNRESPONSIVE, PALE & UNABLE TO OBTAIN A BLOOD PRESSURE. WAS NOTED THAT UPON MOVING CLOTHES TO REVIEW CENTRAL VENOUS TUNNELLED DIALYSIS CATHETER (TCVC) THAT THE VENOUS LINE CONNECTION HAD BECOME DETACHED AND THERE WAS AN ACCUMULATION OF BLOOD BOTH ON FLOOR AND UNDER CLIENT, AND UNFORTUNATELY THE PATIENT PASSED AWAY.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 14269706 ↗

Other Catheter, hemodialysis, implanted devices

All Catheter, hemodialysis, implanted devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.