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PROPHYFLEX 2 HANDPIECE 2012 Adverse Event — Malfunction (MDR 3003637274-2020-00009)

PROPHYFLEX 2 HANDPIECE 2012 Adverse Event — Malfunction (MDR 3003637274-2020-00009) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PROPHYFLEX 2 HANDPIECE 2012; Generic name: DENTAL HANDPIECE; Manufacturer: KAVO DENTAL GMBH.

DevicePROPHYFLEX 2 HANDPIECE 2012
Generic nameDENTAL HANDPIECE
ManufacturerKAVO DENTAL GMBH
Report number3003637274-2020-00009
Event typeMalfunction
Product problemN
Date received2020-04-28
Report sourceDISTRIBUTOR, USER FACILITY
NarrativeUP TO NOW WE DID NOT RECEIVE THE PRODUCT FOR ANALYSIS AND WE DID NOT GET FURTHER INFORMATION REGARDING THE PATIENT OUTCOME. ALSO THE SERIAL NUMBER OF THE PRODUCT HAS NOT BEEN SUPPLIED. AS THE CUSTOMER HAS SEVERAL OF THESE HANDPIECES WE CAN JUST ESTIMATE THE AGE. AS ALL OF THEM HAVE BEEN PRODUCED IN 1998 JUST THE MONTH IS NOT CLEAR - WHICH MAKES NO DIFFERENCE REGARDING THE INCIDENT. TO AVOID SUCH I
SourceopenFDA MAUDE (device adverse events)

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