International Medical Devices Database

Manufacturer Address
Sedecal USA, Inc., 230 Lexington Dr, Buffalo Grove IL 60089-6930
Manufacturer Parent Company (2017)
Sociedad Española De Electromedicina Y Calidad Sa
Source
USFDA
1 Event
- Recall of Device Recall Sedecal SA Mobile Diagnost w DR xray system

One device in the database

Device Recall Sedecal SA Mobile Diagnost w DR xray system

Model / Serial
System Code 712001
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
US Distribution - TX, OH, NY, MD, IN, PA, DE, WA, NH, AZ, GA, NC, UT, VT, CA, LA, NJ, MN, FL, WI, HI, IA, MA, ME, TN, CT, ID, MI, AR and KS.
Product Description
Sedecal SA Mobile Diagnost w DR x-ray system

One manufacturer with a similar name

Learn more about the data here

Sedecal USA, Inc.

Manufacturer Address
Sedecal USA, Inc., 2910 N. Arlington Heights Rd, Arlington Heights IL 60004
Source
USFDA

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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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