RAY-BAN OLYMPIAN III W 0741

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05 report with the FDA on 1998-12-07 for RAY-BAN OLYMPIAN III W 0741 manufactured by Bausch & Lomb, Inc..

Event Text Entries

[17110322] Consumer alleges an injury requiring medical treatment, caused by her sunglasses when she was hit in the face with a softball.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1643383-1998-00006
MDR Report Key201189
Report Source04,05
Date Received1998-12-07
Date of Report1998-11-19
Date of Event1997-11-20
Date Mfgr Received1997-11-20
Date Added to Maude1998-12-14
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
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameRAY-BAN
Generic NameSUNGLASSESS
Product CodeHQY
Date Received1998-12-07
Returned To Mfg1997-11-20
Model NumberOLYMPIAN III
Catalog NumberW 0741
Lot NumberNA
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeNA
Device Eval'ed by Mfgr*
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key195424
ManufacturerBAUSCH & LOMB, INC.
Manufacturer Address5335 CASTROVILLE RD. SAN ANTONIO TX 78227 US
Baseline Brand NameRAY-BAN SUNGLASSES
Baseline Generic NameSUNGLASSES
Baseline Model NoOLYMPIAN III
Baseline Catalog NoW0741
Baseline IDNA
Baseline Device FamilyNA
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 1998-12-07

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