FDA Adverse Event Injury Summary report: N

ATALANTE X

MDR report key: 23851368 · Received December 19, 2025

Report

Report Number
3015000676-2025-00002
Event Type
Injury
Date Received
December 19, 2025
Date of Event
November 19, 2025
Report Date
December 19, 2025
Manufacturer
WANDERCRAFT SAS
Product Code
PHL
UDI-DI
3665965000075
PMA / PMN Number
K232077
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

THE INCIDENT OCCURRED DURING A THERAPIST TRAINING SESSION IN FRANCE, SPECIFICALLY DURING THE PATIENT SESSION (FINAL SESSION OF THE TRAINING PROGRAM). AT THE TIME OF THE EVENT, THE TRAINEE OPERATOR DID NOT FOLLOW ESTABLISHED TRAINING INSTRUCTIONS AND SAFETY PROCEDURES FOR SECURING THE EXOSKELETON TO THE OVERHEAD SAFETY RAIL. SPECIFICALLY, THE OPERATOR ATTACHED THE DEVICE TO THE RAIL USING A THIN METAL CABLE INTENDED SOLELY TO PREVENT THE SWIVEL RETAINING SCREWS FROM LOOSENING, RATHER THAN USING THE DESIGNATED SWIVEL HOOK, WHICH IS THE CORRECT AND LOAD-BEARING ATTACHMENT POINT. A TEMPORARY IMBALANCE WAS NOTED DURING THE SESSION, WITHOUT INDICATION OF DEVICE MALFUNCTION. THE EVENT OCCURRED IN A CONTEXT OF INADEQUATE ADHERENCE TO ESTABLISHED OPERATING PROCEDURES AND REDUCED OPERATOR VIGILANCE DURING DEVICE SETUP AND USE. AS THE METAL CABLE IS NOT DESIGNED TO SUPPORT THE WEIGHT OF THE DEVICE, IT FAILED UNDER LOAD, RESULTING IN A LATERAL FALL OF THE EXOSKELETON. NO INJURIES WERE REPORTED (NO BRUISING, FRACTURES, OR OTHER HARM). THE PATIENT WAS REASSESSED SEVERAL DAYS LATER, AND THE ABSENCE OF INJURY WAS CONFIRMED. WHILE THE OUTCOME WAS BENIGN, THE INCIDENT HAD THE POTENTIAL TO RESULT IN SERIOUS INJURY. HUMAN FACTORS / ABNORMAL USE CONDITIONS: THE INCIDENT OCCURRED IN A CONTEXT OF OPERATOR NON-COMPLIANCE WITH TRAINING INSTRUCTIONS AND REDUCED SITUATIONAL AWARENESS DURING DEVICE SETUP. THE OPERATOR MISIDENTIFIED THE CORRECT ATTACHMENT POINT DESPITE PRIOR TRAINING AND CLEAR INSTRUCTIONS PROVIDED IN BOTH THE USER MANUAL AND THE TRAINING PROGRAM. THE METAL CABLE USED IS VISIBLY THINNER AND MECHANICALLY UNSUITABLE AS A LOAD-BEARING CONNECTION. HOWEVER, IT CURRENTLY LACKS EXPLICIT DESIGN CUES (E.G., COLOR CODING, LABELING, OR A PHYSICAL DETERRENT) TO PREVENT IT FROM BEING MISTAKENLY USED AS THE PRIMARY ATTACHMENT POINT, WHICH MAY INCREASE THE LIKELIHOOD OF MISUSE UNDER CONDITIONS OF INATTENTION OR DEVIATION FROM STANDARD OPERATING PROCEDURES. ALTHOUGH THE SAFETY SYSTEM AS DESCRIBED IN DETAIL IN THE USER MANUAL, IS SAFE WHEN USED AS INTENDED, AND SAFETY PROCEDURES ARE THOROUGHLY ADDRESSED DURING TRAINING PARTICULARLY REGARDING CORRECT ATTACHMENT POINTS, THIS EVENT HIGHLIGHTS OPPORTUNITIES TO FURTHER IMPROVE USABILITY AND ERROR-PROOFING TO MITIGATE THE RISK OF IMPROPER USE, ESPECIALLY IN SITUATIONS WHERE ESTABLISHED PROCEDURES ARE NOT STRICTLY FOLLOWED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
258997 ATALANTE X POWERED LOWER LIMB EXOSKELETON PHL WANDERCRAFT SAS DMR ATA 2.4 07/082030 3665965000075

Patients

Seq Age Sex Outcome Treatment
1 51 YR Male