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INDURA Adverse Event — Injury (MDR 6000030-2008-00719)

INDURA Adverse Event — Injury (MDR 6000030-2008-00719) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INDURA; Manufacturer: RICE CREEK MANUFACTURING; Report number: 6000030-2008-00719.

DeviceINDURA
ManufacturerRICE CREEK MANUFACTURING
Report number6000030-2008-00719
Event typeInjury
Product problemN
Date received2008-02-15
Report sourceConsumer, Health Professional
NarrativeIT WAS REPORTED THAT THE PATIENT EXPERIENCED RINGING IN HER RIGHT EAR, POUNDING IN HER HEAD, LOSS OF THE MOTOR SKILLS IN HER LEFT ARM. SHE REPORTED THAT SHE CANNOT HOLD A CAN OF POP OR OPEN THE DOOR WITH A KNOB. SHE REPORTED HER LEFT ARM WAS A PURPLISH/REDDISH COLOR. SHE REPORTED THE BACK OF HER HEAD FELT STIFF AND VERY HEAVY ALL THE TIME; SHE CANNOT HOLD IT UP FOR VERY LONG TIME AND FELT A SHARP
SourceopenFDA MAUDE (device adverse events)

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