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LORAD Adverse Event — Malfunction (MDR 1220984-1997-00012)

LORAD Adverse Event — Malfunction (MDR 1220984-1997-00012) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LORAD; Generic name: RADIOLOGRAPHIC-MAMMOGRAPHY; Manufacturer: LORAD CORP..

DeviceLORAD
Generic nameRADIOLOGRAPHIC-MAMMOGRAPHY
ManufacturerLORAD CORP.
Report number1220984-1997-00012
Event typeMalfunction
Product problemY
Date received1997-06-23
Report sourceCompany representation
NarrativeC-ARM ROTATED WITH PT UNDER COMPRESSION.
SourceopenFDA MAUDE (device adverse events)

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