International Medical Devices Database

Manufacturer Address
Standard Imaging Inc., 7601 Murphy Rd, Middleton WI 53562
Source
USFDA
1 Event
- Recall of Device Recall Exradin

One device in the database

Device Recall Exradin

Model / Serial
Serial numbers XA030414, XA030413, XA030412, XA030411, XA030281, XA030225, XA030224, XA023341, XA023251, XA022101, XA021649, XA021645, XA021642, XA021641, XA020741, XA020176, XA020171, XA020143, XA013118, XA012743, XA012741, XA011444, XA392, 390, and 345
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
The product was shipped to 24 hospitals located nationwide in the United States.
Product Description
Exradin A12 Ionization Chamber

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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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Standard Imaging Inc.

One device in the database

Device Recall Exradin