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FEMUR CEMENTED POSTERIOR STABILIZED (PS) STANDARD LEFT SIZE 4 Adverse Event — Malfunction (MDR 3007963827-2020-00122)

FEMUR CEMENTED POSTERIOR STABILIZED (PS) STANDARD LEFT SIZE 4 Adverse Event — Malfunction (MDR 3007963827-2020-00122) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FEMUR CEMENTED POSTERIOR STABILIZED (PS) STANDARD LEFT SIZE 4; Generic name: PROSTHESIS, KNEE; Manufacturer: ZIMM

DeviceFEMUR CEMENTED POSTERIOR STABILIZED (PS) STANDARD LEFT SIZE 4
Generic namePROSTHESIS, KNEE
ManufacturerZIMMER ORTHOPAEDIC MFG. LTD.
Report number3007963827-2020-00122
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, DISTRI
NarrativeNO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
SourceopenFDA MAUDE (device adverse events)

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