CLEAR CARE PLUS H14124-1215

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-22 for CLEAR CARE PLUS H14124-1215 manufactured by Alcon Research, Llc..

MAUDE Entry Details

Report NumberMW5090576
MDR Report Key9225155
Date Received2019-10-22
Date of Report2019-10-19
Date of Event2019-10-13
Date Added to Maude2019-10-23
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCLEAR CARE PLUS
Generic NameACCESSORIES, SOFT LENS PRODUCTS
Product CodeLPN
Date Received2019-10-22
Model NumberH14124-1215
Lot Number306045F
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LLC.


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-10-22

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