MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,07 report with the FDA on 2000-08-18 for OPHTHALAS SP manufactured by Alcon-irvine Technology Center.
[166893]
Reporter noted 1. 7w power was selected and fired several times without problem. Suddenly laser delivered a 2. 25w shot, causing a small retinal burn. No intervention reported.
Patient Sequence No: 1, Text Type: D, B5
[203431]
Follow-up indicated pt was followed on a regular basis and this incident had no consequence.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2028159-2000-00200 |
MDR Report Key | 291060 |
Report Source | 01,05,07 |
Date Received | 2000-08-18 |
Date of Report | 2000-07-20 |
Date Mfgr Received | 2000-07-20 |
Date Added to Maude | 2000-08-21 |
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 | 0 |
Manufacturer Contact | NED LUCE |
Manufacturer Street | 6201 SOUTH FREEWAY |
Manufacturer City | FORT WORTH TX 761342099 |
Manufacturer Country | US |
Manufacturer Postal | 761342099 |
Manufacturer Phone | 8175686470 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OPHTHALAS SP |
Generic Name | LASER PHOTOCOAGULATOR |
Product Code | HQB |
Date Received | 2000-08-18 |
Model Number | OPHTHALAS SP |
Catalog Number | OPHTHALAS SP |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 281705 |
Manufacturer | ALCON-IRVINE TECHNOLOGY CENTER |
Manufacturer Address | 15800 ALTON PKWY. IRVINE CA 92618 US |
Baseline Brand Name | OPHTHALAS ARGON/KRYPTON PHOTOCOAGULATOR |
Baseline Generic Name | LASER PHOTOCOAGULATOR |
Baseline Model No | OPHTHALAS SP |
Baseline Catalog No | OPHTHALAS SP |
Baseline ID | NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2000-08-18 |