HOUSE CRABTREE DISSECTOR PICK N1705 83J

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 1997-11-20 for HOUSE CRABTREE DISSECTOR PICK N1705 83J manufactured by Storz Instrument Co..

Event Text Entries

[113423] The tip of the instrument broke off while attempting to remove wax from the pt's ear. There was no pt injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1997-00100
MDR Report Key134489
Report Source05,06
Date Received1997-11-20
Date of Report1997-10-21
Date of Event1997-10-01
Date Facility Aware1997-10-01
Report Date1997-10-21
Date Reported to Mfgr1997-10-21
Date Mfgr Received1997-10-21
Date Added to Maude1997-11-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHOUSE CRABTREE DISSECTOR PICK
Generic NameMICROSURGICAL EAR PICK
Product CodeJYT
Date Received1997-11-20
Model NumberNA
Catalog NumberN1705 83J
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age6 YR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key131419
ManufacturerSTORZ INSTRUMENT CO.
Manufacturer Address499 SOVEREIGN CT. ST LOUIS MO 63011 US
Baseline Brand NameHOUSE CRABTREE DISSECTOR PICK
Baseline Generic NameMICROSURGICAL EAR PICK
Baseline Model NoNA
Baseline Catalog NoN1705 83J
Baseline IDNA
Baseline Device FamilyEAR PICK
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 1997-11-20

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