# FDA recall Z-1739-2025

> **WANDERCRAFT SAS** · Class II · device recall initiated 2025-04-03.

## 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.

## Reason for recall

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

## Distribution

Domestic: PA & NY.

## Key facts

- **Recall number:** Z-1739-2025
- **Recalling firm:** WANDERCRAFT SAS
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-03
- **Report date:** 2025-05-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Paris, N/A, France

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1739-2025

## Citation

> AI Analytics. FDA recall Z-1739-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1739-2025. Source: US FDA. Licensed CC0.

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