CMI - LATERAL 4607

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-05-08 for CMI - LATERAL 4607 manufactured by Stryker Endoscopy-san Jose.

Event Text Entries

[144517485] Additional information will be provided once the investigation has been completed. The device manufacturer date is not known at this time. However, should it become available it will be provided in future reports.
Patient Sequence No: 1, Text Type: N, H10


[144517486] It was reported that the product broke. It was not confirmed if all the broken pieces were retrieved.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002936485-2019-00195
MDR Report Key8592779
Report SourceHEALTH PROFESSIONAL
Date Received2019-05-08
Date of Report2019-09-13
Date of Event2019-04-10
Date Mfgr Received2019-04-10
Date Added to Maude2019-05-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. ANDREA ZENERE
Manufacturer Street5900 OPTICAL COURT
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1STRYKER ENDOSCOPY-SAN JOSE
Manufacturer Street5900 OPTICAL COURT
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal Code95138
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCMI - LATERAL
Generic NameSCAFFOLD, PARTIAL MEDIAL MENISCAL DEFECTS EXTENDING INTO THE RED/WHITE ZONE, RES
Product CodeOLC
Date Received2019-05-08
Returned To Mfg2019-07-13
Catalog Number4607
Lot Number18F538
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ENDOSCOPY-SAN JOSE
Manufacturer Address5900 OPTICAL COURT SAN JOSE CA 95138 US 95138


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-05-08

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