OPHTHALAS SP

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number2028159-2000-00200
MDR Report Key291060
Report Source01,05,07
Date Received2000-08-18
Date of Report2000-07-20
Date Mfgr Received2000-07-20
Date Added to Maude2000-08-21
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 Location0
Manufacturer ContactNED LUCE
Manufacturer Street6201 SOUTH FREEWAY
Manufacturer CityFORT WORTH TX 761342099
Manufacturer CountryUS
Manufacturer Postal761342099
Manufacturer Phone8175686470
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameOPHTHALAS SP
Generic NameLASER PHOTOCOAGULATOR
Product CodeHQB
Date Received2000-08-18
Model NumberOPHTHALAS SP
Catalog NumberOPHTHALAS SP
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key281705
ManufacturerALCON-IRVINE TECHNOLOGY CENTER
Manufacturer Address15800 ALTON PKWY. IRVINE CA 92618 US
Baseline Brand NameOPHTHALAS ARGON/KRYPTON PHOTOCOAGULATOR
Baseline Generic NameLASER PHOTOCOAGULATOR
Baseline Model NoOPHTHALAS SP
Baseline Catalog NoOPHTHALAS SP
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2000-08-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.