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POWER PRO AMBULANCE COT Adverse Event — Malfunction (MDR 0001831750-2020-00609)

POWER PRO AMBULANCE COT Adverse Event — Malfunction (MDR 0001831750-2020-00609) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: POWER PRO AMBULANCE COT; Generic name: STRETCHER, WHEELED; Manufacturer: STRYKER MEDICAL-KALAMAZOO.

DevicePOWER PRO AMBULANCE COT
Generic nameSTRETCHER, WHEELED
ManufacturerSTRYKER MEDICAL-KALAMAZOO
Report number0001831750-2020-00609
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. 1 DEVICE WAS NOT EVALUATED AND THE ISSUE WAS NOT CONFIRMED, AS THE CUSTOMER DID NOT MAKE THE DEVICE AVAILABLE FOR EVALUATION. 7 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; 1 DEVICE HAD A BENT COMPONENT, 1 DEVICE HAD A WORN COMPONENT, 4 DEVICES HAD BROKEN/DAMAGE
SourceopenFDA MAUDE (device adverse events)

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