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Kendall SCD 29525BRecalls & reported problems

Cardinal Health, Inc. · 700 Sequential Compression System · Class 2

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 10884521129627), received between Feb 26, 2020 and Feb 26, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Flare or Flash” (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

  • Flare or Flash1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionFeb 26, 2020Flare or Flash; Flare or Flash

    THE CUSTOMER REPORTED THE DEVICE WAS ATTACHED TO THE END OF THE BED AND WHEN IT WAS SWITCHED ON, THERE WAS A BANG AND A FLASH WHERE THE CABLE CONNECTS TO THE UNIT. THIS RESULTED IN THE MAIN CIRCUIT BREAKER WITHIN THE LOCAL DISTRIBUTION BOARD TRIPPING. THE CUSTOMER ALSO REPORTED THERE WAS AN UNKNOWN PINKISH FLUID DRIPPING FROM THE MAIN CABLE CONNECTED TO THE MACHINE. THE UNIT HAD BEEN IN USE IN THEATER PRIOR TO THIS INCIDENT AND HAD BEEN RETURNED TO THE MATERNITY WARD.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9758796 ↗

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.