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IN TOUCH ZX Adverse Event — Malfunction (MDR 0001831750-2020-00587)

IN TOUCH ZX Adverse Event — Malfunction (MDR 0001831750-2020-00587) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: IN TOUCH ZX; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL-KALAMAZOO.

DeviceIN TOUCH ZX
Generic nameBED, AC-POWERED ADJUSTABLE HOSPITAL
ManufacturerSTRYKER MEDICAL-KALAMAZOO
Report number0001831750-2020-00587
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 NOT EVALUATED, AS THE ISSUE WAS IDENTIFIED AND RESOLVED DURING A TROUBLESHOOTING CALL BETWEEN THE CUSTOMER AND STRYKER TECHNICAL SUPPORT. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE.
SourceopenFDA MAUDE (device adverse events)

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