CONSTELLATION ULTRAVIT PROBE 8065750949

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-12-30 for CONSTELLATION ULTRAVIT PROBE 8065750949 manufactured by Alcon Research, Llc - Houston.

Event Text Entries

[177935234] Investigation including root cause analysis is in progress. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when additional reportable information becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[177935235] A nurse reported the vitrectomy probe was not cutting and the aspiration was working during a vitrectomy procedure. The procedure was completed after the product was replaced with another one. There was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644019-2019-00211
MDR Report Key9532401
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2019-12-30
Date of Report2020-03-16
Date of Event2019-12-09
Date Mfgr Received2020-03-03
Device Manufacturer Date2018-03-20
Date Added to Maude2019-12-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JONATHAN SCHLECH
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8175514979
Manufacturer G1ALCON RESEARCH, LLC - HOUSTON
Manufacturer Street9965 BUFFALO SPEEDWAY
Manufacturer CityHOUSTON TX 77054
Manufacturer CountryUS
Manufacturer Postal Code77054
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameCONSTELLATION ULTRAVIT PROBE
Generic NameVITRECTOMY, INSTRUMENT CUTTER
Product CodeMLZ
Date Received2019-12-30
Model NumberNA
Catalog Number8065750949
Lot Number2126167H
Device Expiration Date2020-01-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LLC - HOUSTON
Manufacturer Address9965 BUFFALO SPEEDWAY HOUSTON TX 77054 US 77054


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-30

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