FDA Recall Open, Classified

Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory functions and mobility exercises, hands-free, in rehabilitation institutions under the supervision of a trained operator.

Recall: Z-1739-2025 · Initiated April 3, 2025

Recall

Recall Number
Z-1739-2025
Event Number
96635
Firm
WANDERCRAFT SAS
FEI Number
3015000676
Product Code
PHL
Status
Open, Classified
Root Cause
Use error
Initiated
April 3, 2025
Posted
May 8, 2025
Address
88 Rue De Rivoli Paris France

Description

Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory functions and mobility exercises, hands-free, in rehabilitation institutions under the supervision of a trained operator.

Reason

Potential for exoskeleton to lose lateral balance and cause patient to fall.

Action

An URGENT SAFETY NOTICE dated 4/3/25 was mailed to consignees. The letter notifies consignees that WANDERCRAFT will be reinforcing their training program for the Atalante X and providing additional instructions by 5/1/25. Until the additional instructions can be provided, users are being instructed to only have certified Atalante X operators maintain the stability of the exoskeleton at all times by keeping at least one hand on the handles throughout the session. Consignees are to share the recall notification with users at their facility and retained for awareness.

Distribution

Domestic: PA & NY.

Quantity

3