STORZ DAVIS MOUTH GAG N7451

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,06 report with the FDA on 1996-09-06 for STORZ DAVIS MOUTH GAG N7451 manufactured by Storz Instrument Company.

Event Text Entries

[27684] During a tonsillectomy procedure, the mechanism that controls the lock on this mouth gag was not working correctly and a crack could be seen. Another gag was used to successfully complete the procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1996-00070
MDR Report Key40653
Report Source00,06
Date Received1996-09-06
Date of Report1996-08-08
Date of Event1996-08-07
Date Facility Aware1996-08-07
Report Date1996-08-08
Date Reported to Mfgr1996-08-08
Date Mfgr Received1996-08-08
Date Added to Maude1996-10-04
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 NameSTORZ DAVIS MOUTH GAG
Generic NameMOUTH GAG
Product CodeKBN
Date Received1996-09-06
Model NumberNA
Catalog NumberN7451
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age1 MO
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key41743
ManufacturerSTORZ INSTRUMENT COMPANY
Manufacturer Address3365 TREE COURT INDUSTRIAL BLVD. ST LOUIS MO 63122 US
Baseline Brand NameSTORZ DAVIS DOUBLE BITE MOUTH GAG
Baseline Generic NameMOUTH GAG
Baseline Model NoNA
Baseline Catalog NoN7451
Baseline IDNA
Baseline Device FamilyMOUTH GAG
Baseline Shelf Life ContainedA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
10 1996-09-06

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