International Medical Devices Database

Manufacturer Address
Biosound Esaote, Inc., 8000 Castleway Drive, Indianapolis IN 46250
Source
USFDA
1 Event
- Recall of Device Recall Caris Plus

One device in the database

Device Recall Caris Plus

Model / Serial
All Caris Plus units with PA220, PA121, PA122, PA023 or PA230 probes. All Megas units with PA122 or PA023 probes.
Distribution
United States and Canada
Product Description
Biosound Caris Plus Ultrasound System with phased array probes, model 7230. || Biosound Megas Ultrasound System with phased array probes, model 7250

One manufacturer with a similar name

Learn more about the data here

Biosound Esaote, Inc.

Manufacturer Address
Biosound Esaote, Inc., 8000 Castleway Dr, Indianapolis IN 46250-1943
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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