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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-1483-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC 1 05/11/2023 Cordis US Corp
Z-1484-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC 1 05/11/2023 Cordis US Corp
Z-1485-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC 1 05/11/2023 Cordis US Corp
Z-1486-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC 1 05/11/2023 Cordis US Corp
Z-1487-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC 1 05/11/2023 Cordis US Corp
Z-1488-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC 1 05/11/2023 Cordis US Corp
Z-1496-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE 1 05/11/2023 Cordis US Corp
Z-1490-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM 1 05/11/2023 Cordis US Corp
Z-1491-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE 1 05/11/2023 Cordis US Corp
Z-1492-2023 - ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE 1 05/11/2023 Cordis US Corp
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