FLYTE SURGICOOL HOOD 0408801400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-11-12 for FLYTE SURGICOOL HOOD 0408801400 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[127135329] Device not returned.
Patient Sequence No: 1, Text Type: N, H10


[127135330] It was reported that during a surgical procedure at the user facility, patient fluid soaked through the hood. The procedure was completed successfully with the same device without a clinically significant delay; there were no adverse consequences or medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2018-02442
MDR Report Key8060457
Date Received2018-11-12
Date of Report2018-11-12
Date of Event2018-10-23
Date Mfgr Received2018-10-23
Date Added to Maude2018-11-12
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 NameFLYTE SURGICOOL HOOD
Generic NameHOOD, SURGICAL
Product CodeFXY
Date Received2018-11-12
Catalog Number0408801400
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-12

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