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Kendall SCD U29525Recalls & reported problems

Cardinal Health, Inc. · KENDALL SCD 700 CONTROLLER US POWER · Class 2

Adverse event reports
7
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10884521129634), received between Nov 1, 2017 and Nov 1, 2017 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Split” (5 reports).

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

  • Split5
  • Temperature Problem2

Patient problems

  • No Information5
  • No Patient Involvement2

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 1, 2017Temperature Problem; Temperature Problem

    ACCORDING TO THE REPORTER, THE UNIT'S FRONT CASE HAS THERMAL DAMAGE.

    Patient problems: No Patient Involvement

    MAUDE report 6994441 ↗
  • MalfunctionNov 1, 2017Split; Split

    UPON TRIAGE IT WAS NOTED THAT THE POWER CORD WAS FOUND TO HAVE A DEEP CUT THAT EXPOSED COPPER WIRES UNDERNEATH

    Patient problems: No Patient Involvement

    MAUDE report 6994186 ↗
  • MalfunctionNov 1, 2017Temperature Problem; Temperature Problem

    UPON TRIAGE, THE UNIT WAS FOUND TO HAVE BURN MARKS ON THE POWER CORD.

    Patient problems: No Information

    MAUDE report 6993992 ↗
  • MalfunctionNov 1, 2017Split; Split

    ACCORDING TO THE REPORTER, THE FRONT CASE WAS BADLY MELTED/SCRATCHED AND THE POWER CORD WAS CUT EXPOSING COPPER WIRES.

    Patient problems: No Information

    MAUDE report 6993630 ↗
  • MalfunctionNov 1, 2017Split; Split

    UPON TRIAGE THE SERVICE TECH FOUND A DAMAGED POWER CORD WITH EXPOSED COPPER.

    Patient problems: No Information

    MAUDE report 6993546 ↗
  • MalfunctionNov 1, 2017Split; Split

    THE CUSTOMER REPORTS THE UNIT IS DAMAGED. UPON TRIAGE, THE SERVICE TECHNICIAN NOTED THAT THE POWER CORD HAS EXPOSED COPPER WIRES.

    Patient problems: No Information

    MAUDE report 6993491 ↗
  • MalfunctionNov 1, 2017Split; Split

    THE UNIT WAS RETURNED WITH NO COMPLAINT LISTED. UPON TRIAGE, THE FOLLOWING ISSUE WAS FOUND: DAMAGED POWER CORD WITH EXPOSED COPPER.

    Patient problems: No Information

    MAUDE report 6993037 ↗

Other SLEEVE, LIMB, COMPRESSIBLE devices

All SLEEVE, LIMB, COMPRESSIBLE devices →

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