Wandercraft
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (2)
- Wandercraft Incorporated FEI 3034724466 · NY
- WANDERCRAFT FEI 3015000676 · FR
Recalls & enforcement
- Class IIOngoing2025-04-03Potential for exoskeleton to lose lateral balance and cause patient to fall.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Wandercraft — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10087464-wandercraft/
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