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Kendall SCD 74022 (UDI 10192253016154)Recalls & reported problems

Cardinal Health 200, LLC · Kendall SCD Sequential Compression Comfort Sleeves, Knee Length, Medium · Class 2

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 10192253016154), received between Jun 23, 2022 and Jun 23, 2022 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Burn(s)1
  • Skin Inflammation/ Irritation1

Recent adverse event reports

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

  • InjuryJun 23, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE CUSTOMER REPORTED THAT ALCARE STOCKINGS AND SCD700 COMFORT SLEEVES WERE ATTACHED TO THE PATIENT WHO WAS TRANSPORTED BY EMERGENCY AMBULANCE DUE TO HEAT STROKE ON 06/03 AND ON 06/05 FIST-SIZED SKIN TISSUE TROUBLE (INFLAMMATION OF THE SKIN) WAS CONFIRMED ON THE LOWER LIMBS/CALF. THE SYMPTOMS WERE CONFIRMED AS LOW TEMPERATURE BURNS. WORSENING/DETERIORATION OF THE AFFECTED AREA WAS SEEN AND HOSPITALIZATION WAS EXTENDED. PHOTOS OF THE AFFECTED AREA WERE REQUESTED BUT ARE NOT AVAILABLE. THE PRODUCT WAS DISCARDED AT THE HOSPITAL AND NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: Burn(s); Skin Inflammation/ Irritation

    MAUDE report 14790864 ↗

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.