Medical Device Recalls
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1 result found
Recall Number: Z-2330-2026 |
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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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| CGuard® Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040 | 2 | 06/05/2026 |
FEI # 3032814119 INSPIREMD Inc |
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