BIOFINITY TORIC (COMFILCON A)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-03-17 for BIOFINITY TORIC (COMFILCON A) manufactured by Coopervision Manufacturing, Ltd..

MAUDE Entry Details

Report Number9614392-2020-00005
MDR Report Key9842297
Report SourceCONSUMER
Date Received2020-03-17
Date of Report2020-03-17
Date Mfgr Received2020-02-16
Device Manufacturer Date2019-09-18
Date Added to Maude2020-03-17
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. MELISSA TORPEY
Manufacturer Street5870 STONERIDGE DRIVE SUITE 1
Manufacturer CityPLEASANTON, CA
Manufacturer CountryUS
Manufacturer Phone7569874
Manufacturer G1COOPERVISION MANUFACTURING, LTD.
Manufacturer StreetSOUTH POINT HAMBLE UNIT 2
Manufacturer CitySOUTHAMPTOM, HAMPSHIRE SO314RF
Manufacturer CountryUK
Manufacturer Postal CodeSO31 4RF
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOFINITY TORIC (COMFILCON A)
Generic NameBIOFINITY TORIC (COMFILCON A)
Product CodeLPM
Date Received2020-03-17
Returned To Mfg2020-03-01
Lot Number12607000047006
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCOOPERVISION MANUFACTURING, LTD.
Manufacturer AddressSOUTH POINT HAMBLE UNIT 2 SOUTHAMPTOM, HAMPSHIRE SO314RF UK SO31 4RF


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-17

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