RAY-BAN DADDYO W2688

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 1999-07-07 for RAY-BAN DADDYO W2688 manufactured by Bausch & Lomb Inc..

Event Text Entries

[15032952] Consumer alleges an accident caused by his sunglasses where one of the temples snapped back into his eye while he was removing them causing injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1643383-1999-00002
MDR Report Key231541
Report Source04,05
Date Received1999-07-07
Date of Report1998-11-10
Date of Event1998-03-12
Date Mfgr Received1999-05-11
Date Added to Maude1999-07-15
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 NameSUNGLASS
Product CodeHQY
Date Received1999-07-07
Returned To Mfg1999-01-01
Model NumberDADDYO
Catalog NumberW2688
Lot NumberNA
ID Number*
OperatorLAY USER/PATIENT
Device Availability*
Device AgeNA
Device Eval'ed by Mfgr*
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key224438
ManufacturerBAUSCH & LOMB INC.
Manufacturer Address5335 CASTROVILLE RD. SAN ANTONIO TX 78227 US
Baseline Brand NameRAY-BAN SUNGLASSES
Baseline Generic NameSUNGLASSES
Baseline Model NoDADDYO
Baseline Catalog NoW2688
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 1999-07-07

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