Incident · Recall
Wandercraft recalls Atalante X self-balancing exoskeleton over a lateral-balance issue that can cause patient falls
Wandercraft initiated a recall of its Atalante X hands-free self-balancing exoskeleton over a lateral-balance condition that could lead to a patient fall during use. Source: FDA device recall Z-1739-2025, accessdata.fda.gov (recall code PHL).
Occurred 2025-04-03 · Wandercraft Atalante X at Paris · Wandercraft · Paris · Exoskeletons · Investigated by FDA
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Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09
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Last reviewed 2026-08-09
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