---
title: "Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory... — FDA record Z-1739-2025 | Is It on Recall"
description: "Potential for exoskeleton to lose lateral balance and cause patient to fall."
url: https://isitonrecall.com/recall/fda-device-z-1739-2025-atalante-x-powered-exoskeleton-atalante-x-is-intended-to-perform-ambulatory-functions-and-mobility-e/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory functions and mobility exercises, hands... — FDA record Z-1739-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 3, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Potential for exoskeleton to lose lateral balance and cause patient to fall.
- **Classification**: Class II
- **Recalling firm**: WANDERCRAFT SAS
- **Quantity**: 3
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1739-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1739-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI: (01)3665965000129(21)V5\_ABP(11)AA06JJ, (01)3665965000129(21)V5\_ACH(11)AA09JJ, (01)3665965000129(21)V5\_ADO(11)AA02JJ. No model or serial number. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic: PA & NY.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)

## Dates in the source

- **Report date**: May 14, 2025
- **Recall initiation date**: Apr 3, 2025
- **Center classification date**: May 8, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1739-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [WANDERCRAFT SAS records](https://isitonrecall.com/brand/wandercraft-sas/)