STORZ SCHIOETZ TONOMETER E5754

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 1998-04-06 for STORZ SCHIOETZ TONOMETER E5754 manufactured by Storz Instrument Co..

Event Text Entries

[124937] A lawsuit was filed whereby the plaintiff alleges that this device was defective and precluded the physician from diagnosing and treating the plaintiff in a timely manner.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1932180-1998-00019
MDR Report Key161181
Report Source06
Date Received1998-04-06
Date of Report1998-03-23
Date of Event1996-06-02
Report Date1998-03-23
Date Reported to Mfgr1998-03-23
Date Mfgr Received1998-03-23
Date Added to Maude1998-04-08
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 SCHIOETZ TONOMETER
Generic NameMANUAL TONOMETER
Product CodeHKY
Date Received1998-04-06
Model NumberNA
Catalog NumberE5754
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeUNKNOWN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key156946
ManufacturerSTORZ INSTRUMENT CO.
Manufacturer Address499 SOVEREIGN CT. ST LOUIS MO 63011 US
Baseline Brand NameSTORZ SCHIOTZ TONOMETER
Baseline Generic NameMANUAL TONOMETER
Baseline Model NoNA
Baseline Catalog NoE5754
Baseline IDNA
Baseline Device FamilyTONOMETER
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Deathisabilit 1998-04-06

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