Paris, N/A, France
WANDERCRAFT SAS recalls
1 recall recorded since 2018, most recently on 3 April 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 3 April 2025
- Reason
- Potential for exoskeleton to lose lateral balance and cause patient to fall.
- Distribution
- Domestic: PA & NY.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1739-2025
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.