Devices

Cordis PRECISE PRO RX Nitinol Stent System (Carotid)

Model / Serial
Cordis PRECISE PRO RX Nitinol Stent System (Carotid) Multiple Catalogue Numbers affectedMultiple Lot Numbers affectedARTG Number: 149399
Product Classification
Cardiovascular Devices
Manufacturer
Johnson & Johnson Medical Pty Ltd
1 Event
- Recall of Cordis PRECISE PRO RX Nitinol Stent System (Carotid)

Manufacturer

Johnson & Johnson Medical Pty Ltd

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
DHTGA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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