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SROM TRI BAND CONE REAMER 19 Adverse Event — Malfunction (MDR 1818910-2020-11320)

SROM TRI BAND CONE REAMER 19 Adverse Event — Malfunction (MDR 1818910-2020-11320) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SROM TRI BAND CONE REAMER 19; Generic name: HIP INSTRUMENTS : REAMERS; Manufacturer: DEPUY ORTHOPAEDICS INC US.

DeviceSROM TRI BAND CONE REAMER 19
Generic nameHIP INSTRUMENTS : REAMERS
ManufacturerDEPUY ORTHOPAEDICS INC US
Report number1818910-2020-11320
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativePRODUCT COMPLAINT #: (B)(4). IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.
SourceopenFDA MAUDE (device adverse events)

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