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UNKNOWN HIP FEMORAL STEM Adverse Event — Injury (MDR 1818910-2020-11349)

UNKNOWN HIP FEMORAL STEM Adverse Event — Injury (MDR 1818910-2020-11349) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN HIP FEMORAL STEM; Generic name: HIP FEMORAL STEM; Manufacturer: DEPUY ORTHOPAEDICS INC US.

DeviceUNKNOWN HIP FEMORAL STEM
Generic nameHIP FEMORAL STEM
ManufacturerDEPUY ORTHOPAEDICS INC US
Report number1818910-2020-11349
Event typeInjury
Product problemY
Date received2020-04-27
Report sourceFOREIGN, HEALTH PROFESSIONAL, L
NarrativeDEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH DEPUY SYNTHES HAS NOT BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY FDA, DEPUY SYNTHES OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE DEVICE, DEPUY SYNTHES, OR ITS EMPLOYEES
SourceopenFDA MAUDE (device adverse events)

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