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HEMO-CATH® MC101041PRecalls & reported problems

Medical Components, Inc. · 10F X 15CM HEMO-CATH® SILICONE DOUBLE LUMEN CATHETER SET (CUFF 11CM FROM TIP) · Class 2 · Implant

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884908093261), received between Jul 10, 2017 and Jul 10, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • Renal Failure1

Recent adverse event reports

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

  • InjuryJul 10, 2017Break; Break

    DURING REMOVAL OF PERM-CATH THE CATHETER CUT AND MIGRATED TO THE HEART. IMPLANTED FOR 1 YEAR.

    Patient problems: Renal Failure

    MAUDE report 6698347 ↗

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.