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Sedecal USA Recalls
1 recall on record · June 15, 2016 to June 15, 2016 · Medical Devices
June 15, 2016
Medical Devices
FDA
Sedecal USA, Inc. recalls Sedecal SA Mobile Diagnost w DR x-ray system
Hazard: Due to a software defect, the system may sporadically apply the default x ray exposure parameters for an adult ( patient type : Normal ) even though the patient type " Newborn" was selected and is displayed in the generator control area of the Eleva User Interface.
Sedecal USA Recalls | RecallWatchUSA