T5 HELMET W/ T4 FIBER OPTIC LIGHT 0400675000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2017-05-23 for T5 HELMET W/ T4 FIBER OPTIC LIGHT 0400675000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[75816420] It was reported that during a surgical procedure at the user facility, the light from the helmet disconnected and burned the surgeon's forehead. The procedure was completed successfully without a clinically significant delay or patient involvement. The user facility was not aware of any medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2017-01255
MDR Report Key6586146
Report SourceUSER FACILITY
Date Received2017-05-23
Date of Report2017-05-23
Date of Event2017-05-11
Date Mfgr Received2017-05-11
Device Manufacturer Date2016-04-11
Date Added to Maude2017-05-23
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. CASEY METZGER
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal49001
Manufacturer Phone2693237700
Manufacturer G1STRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal Code49001
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameT5 HELMET W/ T4 FIBER OPTIC LIGHT
Generic NameHELMET, SURGICAL
Product CodeFXZ
Date Received2017-05-23
Returned To Mfg2017-05-16
Catalog Number0400675000
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-23

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