STRYKER 5MM FIBEROPTIC LIGHT CABLE 0233-050-069 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2004-05-19 for STRYKER 5MM FIBEROPTIC LIGHT CABLE 0233-050-069 NA manufactured by Stryker Endoscopy.

Event Text Entries

[344172] The distal end of the cable was not connected to the endoscope, but was resting on the surgical drape, on top of the pt. There was a hole in the drape where it contacted the light cable. The pt was burned at the hole in the drape. The size of the burn was smaller than a dime. The burn was very red around the perimeter with white blistering in center.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2936485-2004-00022
MDR Report Key563232
Report Source07
Date Received2004-05-19
Date of Report2004-04-15
Date of Event2004-03-30
Report Date2004-03-31
Date Mfgr Received2004-04-15
Date Added to Maude2005-01-06
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 Location0
Manufacturer Street5900 OPTICAL CT
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTRYKER 5MM FIBEROPTIC LIGHT CABLE
Generic NameFIBEROPTIC LIGHT CABLE
Product CodeEQH
Date Received2004-05-19
Model Number0233-050-069
Catalog NumberNA
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeUNKNOWN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedU
Device Sequence No1
Device Event Key552960
ManufacturerSTRYKER ENDOSCOPY
Manufacturer Address5900 OPTICAL CT. SAN JOSE CA 95138 US
Baseline Brand NameSTRYKER 5MM X10 FIBEROPTIC CABLE
Baseline Generic NameFIBEROPTIC CABLE
Baseline Model No0233-050-069
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2004-05-19

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