ACUVUE OASYS SOFT CONTACT LENS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-12 for ACUVUE OASYS SOFT CONTACT LENS manufactured by Johnson & Johnson Vision Care, Inc..

MAUDE Entry Details

Report NumberMW5088962
MDR Report Key8888199
Date Received2019-08-12
Date of Report2019-08-08
Date of Event2019-07-30
Date Added to Maude2019-08-13
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameACUVUE OASYS SOFT CONTACT LENS
Generic NameLENS, CONTACT, (DISPOSABLE)
Product CodeMVN
Date Received2019-08-12
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerJOHNSON & JOHNSON VISION CARE, INC.
Manufacturer AddressJACKSONVILLE FL 32256 US 32256


Patients

Patient NumberTreatmentOutcomeDate
101. Deathisabilit 2019-08-12

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