China NMPA Product Recall - Arterial and Venous Cannula

China NMPA product recall for Arterial and Venous Cannula by Medtronic Inc. published November 13, 2024. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) announced on November 13, 2024, a voluntary Clas

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Record Information

Company

Medtronic Inc.

Inspection Date

Unknown Date

Product Type

ID: 981d0144-f6ee-4bac-8f77-55f69326255d

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