KARL STORZ 12060C

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2009-12-31 for KARL STORZ 12060C manufactured by Karl Storz Gmbh & Co. Kg.

Event Text Entries

[1275188] Allegedly, during an esophagoscopy the pt's esophagus was perforated; the perforation was repaired and pt was released after one week in hospital after doctor confirmed area healed. Later, the pt returned to the hospital and it was found that the repair had broken. Doctor repaired again.
Patient Sequence No: 1, Text Type: D, B5


[8424587] The 12060c was examined and found to be in good working condition and within specifications. There was no damage noted on product.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9610617-2009-00040
MDR Report Key1582691
Report Source06
Date Received2009-12-31
Date of Report2009-12-29
Date of Event2009-08-06
Date Facility Aware2009-12-02
Report Date2009-12-29
Date Reported to FDA2009-12-29
Date Reported to Mfgr2009-12-29
Device Manufacturer Date2009-04-01
Date Added to Maude2011-03-30
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 StreetMITTELSTRASSE 8 POSTFACH 230
Manufacturer CityTUTTLINGEN 78503
Manufacturer CountryGM
Manufacturer Postal78503
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKARL STORZ
Generic NameESOPHAGOSCOPE
Product CodeEOX
Date Received2009-12-31
Model Number12060C
Catalog Number12060C
Lot NumberDB
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age2 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerKARL STORZ GMBH & CO. KG
Manufacturer AddressTUTTLINGEN GM


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2009-12-31

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