InjuryITQ
DONJOY
Received Jul 14, 2026 · Event occurred Jul 31, 2025
Report 9616086-2026-00026 · MDR key 25819839
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Muscle/Tendon Damage
Narrative
Additional Manufacturer Narrative
IT WAS REPORT THAT THE BRACE WAS TOO TIGHT, CAUSED SORES, AND RESULTED IN "DROP FOOT." HE REPORTEDLY DISCONTINUED USE WITHIN A FEW DAYS AND WAS NOT REFITTED. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION, THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE COULD NOT BE ESTABLISHED. ADDITIONAL REPORTING ON THIS EVENT WILL BE PROVIDED AS A SUPPLEMENTAL REPORT TO THIS DOCUMENT IF MORE INFORMATION BECOMES AVAILABLE.
Description of Event or Problem
IT WAS REPORT THAT THE BRACE WAS TOO TIGHT, CAUSED SORES, AND RESULTED IN "DROP FOOT." HE REPORTEDLY DISCONTINUED USE WITHIN A FEW DAYS AND WAS NOT REFITTED.