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Kendall SCD 73022Recalls & reported problems

Cardinal Health 200, LLC · 73022 SCD Express Knee Length Medium - International · 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 10192253016024), received between Jul 23, 2021 and Jul 23, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • Fluid Discharge1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJul 23, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    CUSTOMER REPORTS: THE CATHETERS LEAK BETWEEN THE ATTACHMENT PART (GREEN CONE AND TUBE). THIS CAUSED GASTRIC JUICE TO LEAK INTO THE AREA OF THE PATIENT'S FACE. FURTHERMORE, THE SUCTION POWER WAS INSUFFICIENT AS A RESULT. THIS LEAKAGE WAS OBSERVED OR REPORTED 3 TIMES IN THE LAST FEW DAYS. ADDITIONAL INFORMATION WAS RECEIVED ON 7/21/21 THAT THE GREEN CONNECTOR WAS DISCONNECTED FROM THE TRANSPARENT TUBE.

    Patient problems: Fluid Discharge; No Clinical Signs, Symptoms or Conditions

    MAUDE report 12222196 ↗

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.