Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-1827-2026 - WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair. | 1 | 04/24/2026 |
FEI # 3021071770 WHILL, INC. |
| Z-1826-2026 - WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair. | 1 | 04/24/2026 |
FEI # 3021071770 WHILL, INC. |
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