Cadense Original Women's R3Recalls & reported problems
Cadense, Inc. · Cadense Originals are adaptive walking shoes specifically designed to help with walking difficulties. They feature patented Variable Friction Technology that allows the foot to glide during swing phase and grip during toe-off, supporting smoother, more confident movement. The lightweight design, wide opening, and velcro closure make them easy to put on and wear throughout the day. Cadense Originals combine thoughtful design and function to support everyday mobility across a variety of indoor and outdoor surfaces. · Class 1
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 00810195430564), received between Oct 25, 2025 and Oct 25, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Inadequate Instructions for Non-Healthcare Professional” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Inadequate Instructions for Non-Healthcare Professional1
Patient problems
- Fall1
- Multiple Fractures1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 25, 2025Inadequate Instructions for Non-Healthcare Professional; Inadequate Instructions for Non-Healthcare Professional
CUSTOMER WAS WEARING CADENSE ORIGINAL SHOES WHILE WORKING AS A CLEANING PERSON AT PANERA BREAD. THE GROUND WAS WET CONCRETE, SLOPING DOWNWARD SLIGHTLY. SHE SLIPPED AND FELL TO THE GROUND, WHICH LED TO A BROKEN ANKLE. SHE CALLED AN AMBULANCE TO HELP HER OFF THE GROUND AND ULTIMATELY GOT SURGERY ON HER ANKLE.
Patient problems: Fall; Multiple Fractures
MAUDE report 23387793 ↗
Other Orthosis, Corrective Shoe devices
- PROCARE 79-95725Djo, LLC · ORTHOSIS, CORRECTIVE SHOE3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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