PHOTONGUIDE, WIDE/FLAT 104015

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-30 for PHOTONGUIDE, WIDE/FLAT 104015 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[146788901] It was reported that during a surgical procedure at the user facility, the photonbuide broke in half. The procedure was completed successfully without a clinically significant delay, adverse consequences, or medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2019-01854
MDR Report Key8655906
Date Received2019-05-30
Date of Report2019-05-30
Date of Event2019-04-29
Date Mfgr Received2019-05-02
Device Manufacturer Date2019-01-17
Date Added to Maude2019-05-30
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. ZACH BAKER
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 Report0

Device Details

Brand NamePHOTONGUIDE, WIDE/FLAT
Generic NameLIGHT, SURGICAL, CARRIER
Product CodeFSZ
Date Received2019-05-30
Catalog Number104015
Lot NumberAB19011701
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-30

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