RAY-BAN SUNGLASSES OUTDOORSMAN W1507

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 1996-10-05 for RAY-BAN SUNGLASSES OUTDOORSMAN W1507 manufactured by Bausch & Lomb, Inc.

Event Text Entries

[22310] Customer alleges an injury when a plug ejected from his gun and broke the lens of his sunglass.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1643383-1996-00001
MDR Report Key41590
Report Source04,05
Date Received1996-10-05
Date of Report1996-10-04
Date of Event1996-03-24
Date Mfgr Received1996-05-04
Date Added to Maude1996-10-10
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 SUNGLASSES
Generic NameSUNGLASS
Product CodeHQY
Date Received1996-10-05
Returned To Mfg1996-05-04
Model NumberOUTDOORSMAN
Catalog NumberW1507
Lot NumberNA
ID Number*
OperatorOTHER
Device AvailabilityR
Device Age*
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key42647
ManufacturerBAUSCH & LOMB, INC
Manufacturer Address5335 CASTROVILLE RD SAN ANTONIO TX 78227 US
Baseline Brand NameRAY-BAN SUNGLASSES
Baseline Generic NameSUNGLASSES
Baseline Model NoOUTDOORSMAN
Baseline Catalog NoW1507
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 1996-10-05

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