FDA Adverse Event Injury Summary report: N

EZ CONTACTS

MDR report key: 20895475 · Received December 6, 2024

Report

Report Number
MW5163458
Event Type
Injury
Date Received
December 6, 2024
Date of Event
October 17, 2024
Report Date
December 6, 2024
Manufacturer
EZCONTACTS USA
Product Code
HQG
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
*

Narratives

Description of Event or Problem · 0

EZ CONTACTS SENT TWO DIFFERENT FRAUDULENT RX VERIFICATION REQUESTS TO (B)(6). REFERENCE #: (B)(4) WAS SENT ON (B)(6)2024 FOR (B)(6) CONTACTS AND REFERENCE #: (B)(4) WAS SENT ON (B)(6)2024 FOR (B)(6) CONTACT LENSES. BOTH OF THESE PRESCRIPTIONS WERE FRAUDULENT. NO CONTACT LENS EXAMINATION WAS DONE. NO CONTACT LENS PRESCRIPTION WAS WRITTEN. THE PATIENT WAS TREATED FOR A MEDICAL EYE CONDITION AND TOLD NOT TO WEAR CONTACT LENSES. UNSUCCESSFUL ATTEMPTS WERE MADE TO CONTACT EZ CONTACTS TO CONFIRM IF THE PATIENT PURCHASED CONTACT LENSES OR NOT FROM THE FRAUDULENT PRESCRIPTIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2150878 EZ CONTACTS LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) HQG EZCONTACTS USA

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown