FDA Adverse Event Malfunction Summary report: N

LENSX LASER SYSTEM

MDR report key: 18765687 · Received February 23, 2024

Report

Report Number
2028159-2024-00273
Event Type
Malfunction
Date Received
February 23, 2024
Date of Event
January 15, 2024
Report Date
March 13, 2024
Manufacturer
ALCON LENSX, INC.
Product Code
OOE
UDI-DI
00380659981623
PMA / PMN Number
K163551
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

H.3., H.6.: INVESTIGATION, INCLUDING ROOT CAUSE ANALYSIS, IS IN PROGRESS. A SUPPLEMENTAL MDR WILL BE FILED AS NECESSARY IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL REPORTABLE INFORMATION BECOMES AVAILABLE. ALCON LENSX (SITE #(B)(4)) IS NO LONGER OPERATIONAL. LENSX MANUFACTURED PRODUCTS ARE MAINTAINED AND INVESTIGATED BY THE ALCON RESEARCH, LTD. IRVINE TECHNOLOGY CENTER SITE #(B)(4)). THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).

Additional Manufacturer Narrative · 0

UPON FURTHER REVIEW THIS COMPLAINT WAS REASSESSED AND CONFIRMED THAT, THIS EVENT DOES NOT MEET CRITERIA FOR REPORTING AS A REPORTABLE MALFUNCTION AS THE SYSTEM DISPLAYED RADIO FREQUENCY IDENTIFICATION DEVICE ERROR AND DEVICE NOT WORKING BEFORE SURGERY. NO FURTHER REGULATORY REPORTS REQUIRED. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).

Description of Event or Problem · 0

A NON-HEALTHCARE PROFESSIONAL THAT THE SYSTEM DISPLAYED RADIO FREQUENCY IDENTIFICATION DEVICE ERROR AND DEVICE WAS NOT WORKING BEFORE SURGERY IN THE UNKNOWN EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
112084 LENSX LASER SYSTEM OPHTHALMIC FEMTOSECOND LASER OOE ALCON LENSX, INC. 550 NA 00380659981623

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown LENSX LASER SYSTEM, PATIENT INTERFACE| LENSX LASER SYSTEM, PI