Devices

Precise Pro RX Nitinol Stent System (Carotid)

Model / Serial
Product Description
Medical Device Safety Alert: Cordis Precise Pro RX Nitinol Stent System (Carotid)
Manufacturer
Cordis Corporation
1 Event
- Safety Alert for Precise Pro RX Nitinol Stent System (Carotid)

Manufacturer

Cordis Corporation

Manufacturer Parent Company (2017)
Cardinal Health
Source
DH

One device with a similar name

Learn more about the data here

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

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

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.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)