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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2325-2026 - Brand Name: CGuard® Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830 2 06/05/2026 FEI # 3032814119
INSPIREMD Inc
Z-2326-2026 - Brand Name: CGuard® Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840 2 06/05/2026 FEI # 3032814119
INSPIREMD Inc
Z-2330-2026 - CGuard® Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040 2 06/05/2026 FEI # 3032814119
INSPIREMD Inc
Z-2328-2026 - Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940 2 06/05/2026 FEI # 3032814119
INSPIREMD Inc
Z-2329-2026 - CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030 2 06/05/2026 FEI # 3032814119
INSPIREMD Inc
Z-2327-2026 - CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930 2 06/05/2026 FEI # 3032814119
INSPIREMD Inc
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