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Kendall SCD 73011Recalls & reported problems

Cardinal Health, Inc. · Express Sleeves,Thigh Length, Small · 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 30884521051601), received between Nov 15, 2018 and Nov 15, 2018 — 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

  • Nerve Damage1

Recent adverse event reports

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

  • InjuryNov 15, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE CUSTOMER STATES THE PATIENT HAD A KNOWN CASE DIVERTICULITIS POST EXPLORATORY LAPAROSCOPY WITH LYSIS ADHESION SINCE (B)(6) 2018. THE PATIENT HAD BEEN ON SCD SINCE OPERATION DATE; 8 DAYS LATER ((B)(6) 2018) HE GOT FOOT DROP AND THE NEUROLOGIST HAD BEEN CONSULTED. AFTER INVESTIGATION, THE NEUROLOGIST DECIDED THAT THE NERVE WHICH LIED ON HIS LEGS WAS COMPRESSED BY SCD AND CAUSED FOOT DROP.

    Patient problems: Nerve Damage

    MAUDE report 8074646 ↗

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.