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Split Cath® III ASPC32-3Recalls & reported problems

Medical Components, Inc. · 14F X 32CM SPLIT CATH® III CATHETER SET (CUFF 27CM FROM TIP) · Class 2 · Implant

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 00884908003857), received between Dec 5, 2019 and Dec 5, 2019 — classified as 1 malfunction.

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

  • No Information1

Recent adverse event reports

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

  • MalfunctionDec 5, 2019Disconnection; Disconnection

    DURING DIALYSIS, "THE TUBING CONNECTION BECAME UNSECURE FROM THE LUMEN OF DIALYSIS CATHETER".

    Patient problems: No Information

    MAUDE report 9415469 ↗

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