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STANDARD MODEL BED FL28EX5 Adverse Event — Malfunction (MDR 0001831750-2020-00558)

STANDARD MODEL BED FL28EX5 Adverse Event — Malfunction (MDR 0001831750-2020-00558) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: STANDARD MODEL BED FL28EX5; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL-KALAMAZOO.

DeviceSTANDARD MODEL BED FL28EX5
Generic nameBED, AC-POWERED ADJUSTABLE HOSPITAL
ManufacturerSTRYKER MEDICAL-KALAMAZOO
Report number0001831750-2020-00558
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE
NarrativeTHIS MDR IS A CONSOLIDATION OF RECORDS SUMMARIZED AS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. THE DEVICE IS PENDING EVALUATION. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE.
SourceopenFDA MAUDE (device adverse events)

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