BIOMEDICS TORIC (OCUFILCON D)

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 2020-03-24 for BIOMEDICS TORIC (OCUFILCON D) manufactured by Coopervision Manufacturing Puerto Rico, Llc.

MAUDE Entry Details

Report Number2640128-2020-00002
MDR Report Key9874018
Report SourceCONSUMER
Date Received2020-03-24
Date of Report2020-03-24
Date Mfgr Received2020-02-20
Date Added to Maude2020-03-24
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 PUERTO RICO, LLC
Manufacturer Street500 ROAD 584 LOT 7
Manufacturer CityAMUELAS INDUSTRIAL PARK, JUANA DIAZ 00795
Manufacturer Country*
Manufacturer Postal Code00795
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOMEDICS TORIC (OCUFILCON D)
Generic NameBIOMEDICS TORIC (OCUFILCON D)
Product CodeLPL
Date Received2020-03-24
Lot Number815552526110
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOPERVISION MANUFACTURING PUERTO RICO, LLC
Manufacturer Address500 ROAD 584 LOT 7 AMUELAS INDUSTRIAL PARK, JUANA DIAZ 00795 * 00795


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-24

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