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BELL-HORN 11300XL-SHORTRecalls & reported problems

Djo, LLC · ANTIEMB 18MMHG KN CT BLACK XL/SHORT · Class 2

Data updated Oct 18, 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 00888912223874), received between Jul 21, 2017 and Jul 21, 2017 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Hypersensitivity/Allergic reaction1

Recent adverse event reports

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

  • InjuryJul 21, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    COMPLAINT RECEIVED THAT ALLEGES "ALLERGIC REACTION TO THE COLOR DIE OF THE STOCKING AND BROKE OUT IN HIVES. PATIENT WAS IN THE HOSPITAL FOR 4 DAYS, OUT OF THE HOSPITAL AND WELL NOW". QUESTIONNAIRE NOT RECEIVED FROM CUSTOMER OR CLINICIAN. DEVICE NOT RETURNED TO MANUFACTURER FOR EVALUATION.

    Patient problems: Hypersensitivity/Allergic reaction

    MAUDE report 6731926 ↗

Other Stocking, medical support (to prevent pooling of blood in legs) devices

All Stocking, medical support (to prevent pooling of blood in legs) devices →

Sources and updates

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