ULTRASONIC PROBE 27093LL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2014-11-03 for ULTRASONIC PROBE 27093LL manufactured by Karl Storz Gmbh & Co..

Event Text Entries

[5226285] Allegedly, during a percutaneous nephrolithotomy procedure on (b)(6) 2014, the tip of the ultrasonic probe fell off inside the patient's kidney; the surgeon was able to remove it with a grasper. Procedure was completed with no injury to patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610617-2014-00054
MDR Report Key4268572
Report Source05,06
Date Received2014-11-03
Date of Report2014-10-02
Date of Event2014-10-02
Date Added to Maude2014-11-26
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 FDA0
Event Location0
Manufacturer ContactSUSIE CHEN
Manufacturer Street2151 E. GRAND AVE
Manufacturer CityEL SEGUNDO CA 902455017
Manufacturer CountryUS
Manufacturer Postal902455017
Manufacturer Phone4242188201
Manufacturer G1KARL STORZ GMBH & CO. KG
Manufacturer StreetMITTELSTRASSE 8
Manufacturer CityTUTTLINGEN
Manufacturer CountryGM
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameULTRASONIC PROBE
Generic NameULTRASONIC PROBE
Product CodeFEO
Date Received2014-11-03
Model Number27093LL
Catalog Number27093LL
Lot Number46360
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerKARL STORZ GMBH & CO.
Manufacturer AddressTUTTLINGEN GM


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2014-11-03

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