China NMPA Product Recall - Medtronic PRO+ Transcatheter Aortic Valve System
China NMPA product recall for Medtronic PRO+ Transcatheter Aortic Valve System by Medtronic Inc. published December 23, 2024. Recall level: Level 3 Recall. Medtronic Inc. initiated a voluntary Class III recall of its Transcatheter Aortic Valve System, spec
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China NMPA product recall for Medtronic PRO+ Transcatheter Aortic Valve System by Medtronic Inc. published December 23, 2024. Recall level: Level 3 Recall. Medtronic Inc. initiated a voluntary Class III recall of its Transcatheter Aortic Valve System, spec
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Company
Medtronic Inc.Inspection Date
Unknown Date
Product Type
ID: ec017771-34d6-4260-931d-528017a371d2
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