FDA Adverse Event Injury Summary report: N

ACUVUE OASYS

MDR report key: 5728656 · Received June 13, 2016

Report

Report Number
MW5062870
Event Type
Injury
Date Received
June 13, 2016
Date of Event
June 13, 2016
Report Date
June 13, 2016
Manufacturer
JOHNSON & JOHNSON
Product Code
LPM
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

PT USING (B)(6) TO ORDER CONTACT LENSES WITHOUT A PROPER FIT. FAQ PAGE EVEN REPORTS THAT PT IS NOT ACTUALLY BEING FIT FOR CLS. THIS COULD CAUSE SERIOUS DAMAGE OR BLINDNESS. DATES OF USE: (B)(6) 2016.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
374938 ACUVUE OASYS ACUVUE OASYS LPM JOHNSON & JOHNSON

Patients

Seq Age Sex Outcome Treatment
1 40 YR Disability