International Medical Devices Database

Manufacturer Address
CME America, LLC, 14998 W 6th Ave, Golden CO 80401-6587
Manufacturer Parent Company (2017)
CME America, LLC
Source
USFDA
1 Event
- Recall of Device Recall BodyGuard

One device in the database

Device Recall BodyGuard

Model / Serial
All product with USA36A4.4 version of software affected
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - Nationwide Distribution and VA/military/govt consignees and the country of Canada.
Product Description
BodyGuard 323 pump, models || 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, || 100-603XSA and 100-603XSAP

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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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CME America, LLC

One device in the database

Device Recall BodyGuard