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Kendall SCD 74021 (UDI 10884521130852)Recalls & reported problems

Cardinal Health, Inc. · Sequential Compression Comfort Sleeves,Knee Length, Small · Class 2

All models of Kendall SCD (12)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 10884521130852), received between Jul 12, 2023 and Jul 12, 2023 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Thrombosis/Thrombus1

Recent adverse event reports

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

  • InjuryJul 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE CUSTOMER REPORTED THAT A BLOOD CLOT OCCURRED TO A PATIENT WHO WORE A SMALL-SIZE COMFORT SLEEVE. THE PATIENT'S RIGHT UPPER CALF GOT SWOLLEN, AND THE PATIENT WAS DIAGNOSED WITH A THROMBUS. THE DOCTOR HAS POINTED OUT THAT NOT ENOUGH PRESSURE MIGHT HAVE BEEN APPLIED BECAUSE THE SIZE SMALL WAS SOMEWHAT SMALL FOR THE PATIENT'S LEG. IT IS REPORTED THAT THE NURSE DID NOT PUT THE SLEEVES ON THE PATIENT FIRMLY, THUS IT SEEMS LESS LIKELY THE SLEEVE WAS TIGHTENING THE LOWER LEG. USAGE PERIOD IS 1 DAY.

    Patient problems: Thrombosis/Thrombus

    MAUDE report 17305451 ↗

Other SLEEVE, LIMB, COMPRESSIBLE devices

All SLEEVE, LIMB, COMPRESSIBLE devices →

Sources and updates

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