International Medical Devices Database

Manufacturer Address
Medtronic Cardiac Surgery Technologies, 7601 Northland Drive, Minneapolis MN 55428
Source
USFDA
1 Event
- Recall of Device Recall Medtronic

One device in the database

Device Recall Medtronic

Model / Serial
Lot number 2002080004
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
All of the consignees were in foreign countries in Europe, Asia and Latin America.
Product Description
Medtronic Cardioblate Radio Frequency Ablation Pen, model number 60811C47

One manufacturer with a similar name

Learn more about the data here

Medtronic Cardiac Surgery Technologies

Manufacturer Address
Medtronic Cardiac Surgery Technologies, 7601 Northland Dr N, Minneapolis MN 55428-1088
Source
USFDA

About this database

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

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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.

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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.

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