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MA204 Adverse Event — Malfunction (MDR 0001831750-2020-00559)

MA204 Adverse Event — Malfunction (MDR 0001831750-2020-00559) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MA204; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL-KALAMAZOO.

DeviceMA204
Generic nameBED, AC-POWERED ADJUSTABLE HOSPITAL
ManufacturerSTRYKER MEDICAL-KALAMAZOO
Report number0001831750-2020-00559
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE
NarrativeTHIS MDR IS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. THE DEVICE WAS EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; THERE WAS A BROKEN/DAMAGED COMPONENT. THE DEVICE WAS REPAIRED AND RETURNED. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE.
SourceopenFDA MAUDE (device adverse events)

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