CYSTO-URETHROSCOPE SHEATH 27026BA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-09-14 for CYSTO-URETHROSCOPE SHEATH 27026BA manufactured by Karl Storz Gmbh & Co. Kg Tuttlingen, Germany.

Event Text Entries

[55060014] We evaluated the instrument and confirmed that the tip had come off the instrument. There is a big dent in the middle of the shaft and a smaller one near the distal end. The instrument shows corrosion. It is possible corrosion weakened the metal, or separation may have been caused by stress overload; we cannot confirm.
Patient Sequence No: 1, Text Type: N, H10


[55060015] Allegedly, the doctor was performing a right retrograde pyelogram, ureteral stent placement on a patient when the tip of the sheath separated from the device inside the patient; the doctor retrieved the piece. Hospital states that the procedure was completed with no injury to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610617-2016-00144
MDR Report Key5951483
Date Received2016-09-14
Date of Report2016-08-23
Date of Event2016-08-23
Date Mfgr Received2016-08-23
Device Manufacturer Date2013-11-01
Date Added to Maude2016-09-14
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. SUSIE CHEN
Manufacturer Street2151 E. GRAND AVENUE
Manufacturer CityEL SEGUNDO CA 902455017
Manufacturer CountryUS
Manufacturer Postal902455017
Manufacturer Phone4242188201
Manufacturer G1KARL STORZ GMBH & CO. KG TUTTLINGEN, GERMANY
Manufacturer StreetMITTLESTRASSE 8, 78503
Manufacturer CityTUTTLINGEN, GERMANY,
Manufacturer CountryGM
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCYSTO-URETHROSCOPE SHEATH
Generic NameCYSTO SHEATH
Product CodeODB
Date Received2016-09-14
Returned To Mfg2016-09-07
Model Number27026BA
Catalog Number27026BA
Lot NumberYW
OperatorPHYSICIAN
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerKARL STORZ GMBH & CO. KG TUTTLINGEN, GERMANY
Manufacturer AddressMITTLESTRASSE 8, 78503 TUTTLINGEN, GERMANY, GM


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-09-14

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