Class II

Medical Device Recall: 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

WANDERCRAFT SAS · April 3, 2025

Reason for Recall

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

Product 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.

Distribution

Domestic: PA & NY.

States Affected

NY, PA

Quantity Affected

3

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1739-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

WANDERCRAFT SAS Medical Device Recall: 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 | SafeCheck