'PKG, DEBAKEY FORCEPS' 0250080314

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-25 for 'PKG, DEBAKEY FORCEPS' 0250080314 manufactured by Stryker Endoscopy-san Jose.

Event Text Entries

[112315544] 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


[112315545] It was reported that the product broke inside patient. The broken pieces were successfully removed from patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002936485-2018-00504
MDR Report Key7636030
Date Received2018-06-25
Date of Report2018-09-14
Date of Event2018-05-31
Date Mfgr Received2018-05-31
Date Added to Maude2018-06-25
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. CHESTER REBUGIO
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 Report0

Device Details

Brand Name'PKG, DEBAKEY FORCEPS'
Generic NameENDOSCOPIC GRASPING/CUTTING INSTRUMENT, NON-POWERED
Product CodeOCZ
Date Received2018-06-25
Returned To Mfg2018-07-26
Catalog Number0250080314
Lot Number0143178
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
10 2018-06-25

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