ALCON MICROSURGICAL INSTRUMENTS, CANNULA OPHTHALMIC 8065420120

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-07-30 for ALCON MICROSURGICAL INSTRUMENTS, CANNULA OPHTHALMIC 8065420120 manufactured by Alcon Research, Llc - Alcon Precision Device.

MAUDE Entry Details

Report Number2523835-2019-00345
MDR Report Key8842687
Report SourceHEALTH PROFESSIONAL
Date Received2019-07-30
Date of Report2019-10-18
Date of Event2019-07-09
Date Mfgr Received2019-10-14
Date Added to Maude2019-07-30
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 ContactMS. CINDY MILAM
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8176152231
Manufacturer G1ALCON RESEARCH, LLC - ALCON PRECISION DEVICE
Manufacturer Street714 COLUMBIA AVENUE
Manufacturer CitySINKING SPRING PA 19608
Manufacturer CountryUS
Manufacturer Postal Code19608
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameALCON MICROSURGICAL INSTRUMENTS, CANNULA OPHTHALMIC
Generic NameCANNULA, OPHTHALMIC
Product CodeHMX
Date Received2019-07-30
Model NumberNA
Catalog Number8065420120
Lot NumberASKU
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LLC - ALCON PRECISION DEVICE
Manufacturer Address714 COLUMBIA AVENUE SINKING SPRING PA 19608 US 19608


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-07-30

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