2108 SERIES SAGITTAL BLADE (20.5 X 0.88 X 94.5MM) 2108109001S1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-02-20 for 2108 SERIES SAGITTAL BLADE (20.5 X 0.88 X 94.5MM) 2108109001S1 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[181785565] A follow up report will be filed once the quality investigation is complete. Awaiting return of device to manufacturer.
Patient Sequence No: 1, Text Type: N, H10


[181785566] It was reported that during a surgical procedure, it was noted that the blade broke. It was also reported there were no delays and no adverse consequences as a result of this event. No further information was available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2020-00527
MDR Report Key9733862
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-02-20
Date of Report2020-02-20
Date of Event2020-01-23
Date Mfgr Received2020-01-23
Date Added to Maude2020-02-20
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 ContactMRS. UNA BARRY
Manufacturer StreetINSTRUMENTS DIVISION CARRIGTWOHILL BUS. & TECH PARK
Manufacturer CityCARRIGTWOHILL NA
Manufacturer CountryIE
Manufacturer PostalNA
Manufacturer Phone214532900
Manufacturer G1STRYKER INSTRUMENTS-IRELAND
Manufacturer StreetINSTRUMENTS DIVISION CARRIGTWOHILL BUS. & TECH PARK
Manufacturer CityCARRIGTWOHILL NA
Manufacturer CountryIE
Manufacturer Postal CodeNA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name2108 SERIES SAGITTAL BLADE (20.5 X 0.88 X 94.5MM)
Generic NameBLADE, SAW, GENERAL & PLASTIC SURGERY,SURGICAL
Product CodeGFA
Date Received2020-02-20
Model Number2108109001S1
Catalog Number2108109001S1
Lot NumberUNKNOWN
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 2020-02-20

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.