Medical Device Recalls
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1 result found
Recall Number: Z-1826-2026 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor batt... | 1 | 04/24/2026 |
FEI # 3021071770 WHILL, INC. |
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