WANDERCRAFT SAS: Medical Device Recall in 2025 - (Recall #: Z-1739-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: April 3, 2025

Date Posted: May 14, 2025

Recall Number: Z-1739-2025

Event ID: 96635

Reason for Recall:

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

Status: Ongoing

Product Quantity: 3

Code Information:

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.

Distribution Pattern:

Domestic: PA & NY.

Voluntary or Mandated:

Voluntary: Firm initiated