Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0670-2024 - CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040 | 2 | 01/05/2024 |
FEI # 1000523125 Townsend Design |
| Z-0672-2024 - SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX | 2 | 01/05/2024 |
FEI # 1000523125 Townsend Design |
| Z-0671-2024 - SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, ... | 2 | 01/05/2024 |
FEI # 1000523125 Townsend Design |
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