MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05 report with the FDA on 1997-08-11 for RAY-BAN WAYFARER L1619 manufactured by Bausch & Lomb, Inc..
[69784]
Consumer alleges an injury requiring medical treatment, caused by her sunglasses when her horse reared and hit her with his head.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1643383-1997-00007 |
MDR Report Key | 112685 |
Report Source | 04,05 |
Date Received | 1997-08-11 |
Date of Report | 1997-07-21 |
Date of Event | 1997-03-22 |
Date Mfgr Received | 1997-07-17 |
Date Added to Maude | 1997-08-15 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | RAY-BAN |
Generic Name | SUNGLASS |
Product Code | HQY |
Date Received | 1997-08-11 |
Returned To Mfg | 1997-04-29 |
Model Number | WAYFARER |
Catalog Number | L1619 |
Lot Number | NA |
ID Number | * |
Operator | LAY USER/PATIENT |
Device Availability | Y |
Device Age | NA |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 110617 |
Manufacturer | BAUSCH & LOMB, INC. |
Manufacturer Address | 5335 CASTROVILLE RD. SAN ANTONIO TX 78227 US |
Baseline Brand Name | RAY-BAN SUNGLASSES |
Baseline Generic Name | SUNGLASSES |
Baseline Model No | WAYFARER |
Baseline Catalog No | L1619 |
Baseline ID | NA |
Baseline Device Family | NA |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | Y |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 1997-08-11 |