Class II — WANDERCRAFT SAS
| Recalling firm | Wandercraft |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Potential for exoskeleton to lose lateral balance and cause patient to fall. |
| Product | 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. |
| Quantity | 3 |
| Distribution | Domestic: PA & NY. |
| Initiated | 2025-04-03 |
| Classified | 2025-05-08 |
| Recall number | Z-1739-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — WANDERCRAFT SAS (Z-1739-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96635/
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