← DeviceEvents
HomeDevice Adverse Events

BATTERY RECIPROCATOR II FOR BPL II Adverse Event — Malfunction (MDR 8030965-2020-03119)

BATTERY RECIPROCATOR II FOR BPL II Adverse Event — Malfunction (MDR 8030965-2020-03119) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BATTERY RECIPROCATOR II FOR BPL II; Generic name: MOTOR, SURGICAL INSTRUMENT, AC-POWERED; Manufacturer: DEPUY SYNTHES PRODUCTS LLC.

DeviceBATTERY RECIPROCATOR II FOR BPL II
Generic nameMOTOR, SURGICAL INSTRUMENT, AC-POWERED
ManufacturerDEPUY SYNTHES PRODUCTS LLC
Report number8030965-2020-03119
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, FOREIG
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)

🔍 Search all device adverse events →