Medical Device Recalls
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1 result found
Recall Number: Z-1026-2022 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit... | 2 | 04/29/2022 |
FEI # 3014833750 restor3d Inc. |
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