OPMI 1 MICROSCOPE ON S1 STAND

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2017-04-13 for OPMI 1 MICROSCOPE ON S1 STAND manufactured by Carl Zeiss Meditec Ag (oberkochen).

Event Text Entries

[72807447]
Patient Sequence No: 1, Text Type: N, H10


[72807448] This is case two of two reported from the same customer site. The health care professional (hcp) reported that, the site's technician was plugging the opmi 1 microscope on s1 stand into the power outlet. She received an electric shock when she accidently touched the exposed wire of the pre-damaged power cord (near the connector). The technician was not injured from the event. She did not consult a physician nor did she require any medical treatment.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615010-2017-00004
MDR Report Key6491369
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2017-04-13
Date of Report2017-03-14
Date of Event2017-03-06
Date Mfgr Received2017-09-15
Device Manufacturer Date1990-01-01
Date Added to Maude2017-04-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. WILLIAM GUSTAFSON
Manufacturer StreetCARL ZEISS MEDITEC, INC.
Manufacturer CityDUBLIN CA 94568
Manufacturer CountryUS
Manufacturer Postal94568
Manufacturer Phone9255574689
Manufacturer G1CARL ZEISS MEDITEC AG (OBERKOCHEN)
Manufacturer StreetRUDOLF-EBER-STRASSE 11
Manufacturer CityOBERKOCHEN, BADEN-WUERTTEMBERG 73447
Manufacturer CountryGM
Manufacturer Postal Code73447
Single Use3
Remedial ActionIN
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameOPMI 1 MICROSCOPE ON S1 STAND
Generic NameSURGICAL MICROSCOPE
Product CodeFSO
Date Received2017-04-13
Model NumberNA
Catalog NumberNA
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCARL ZEISS MEDITEC AG (OBERKOCHEN)
Manufacturer AddressRUDOLF-EBER-STRASSE 11 OBERKOCHEN, BADEN-WUERTTEMBERG 73447 GM 73447


Patients

Patient NumberTreatmentOutcomeDate
10 2017-04-13

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