FDA Adverse Event Injury Summary report: N

IDESIGN RS

MDR report key: 16710855 · Received April 11, 2023

Report

Report Number
3012236936-2023-00881
Event Type
Injury
Date Received
April 11, 2023
Date of Event
December 22, 2022
Report Date
April 10, 2023
Manufacturer
AMO MANUFACTURING USA, LLC
Product Code
LZS
UDI-DI
05050474651432
PMA / PMN Number
P930016
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DEVICE EVALUATION: AN APPLICATION SUPPORT MANAGER (ASM) VISITED SITE AND PROVIDED SURGERY SUPPORT. MANUFACTURING RECORDS REVIEW: THE MANUFACTURING RECORDS FOR THE DEVICE WERE REVIEWED. THE PRODUCT WAS MANUFACTURED AND RELEASED ACCORDING TO SPECIFICATION. CONCLUSION: AS A RESULT OF THE INVESTIGATION THERE IS NO INDICATION OF A PRODUCT QUALITY DEFICIENCY AND THE REPORTED ISSUE COULD NOT BE VERIFIED. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC. HAS BEEN SUBMITTED.

Description of Event or Problem · 0

IT WAS REPORTED THAT PATIENT HAD SURGERY ON (B)(6) 2022 AND WAS OVERCORRECTED IN THE LEFT EYE. IDESIGN MANIFEST REFRACTION (MR) -9.12 +2.90 X 100, MR. -8.25 +2.75 97 BEST CORRECTED VISUAL ACUITY (BCVA) 20/20. AN ENHANCEMENT WAS PERFORMED ON (B)(6)2022. IDESIGN MR -.10 +1.14 X79, MR +1.25 SPH. PHYSICIAN ADJ +.50. PATIENT ENDED UP WITH 20/25 UNCORRECTED VISUAL ACUITY (UCVA). NO REFRACTION HAS BEEN DONE AND PATIENT IS NOT DUE TO RETURN FOR ANOTHER 6 MONTHS. NO ADDITIONAL INFORMATION WAS PROVIDED. THIS REPORT IS FOR THE IDESIGN. A SEPARATE REPORT WILL BE FILED FOR THE EXCIMER LASER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
425043 IDESIGN RS EXCIMER LASER SYSTEM LZS AMO MANUFACTURING USA, LLC G301 05050474651432

Patients

Seq Age Sex Outcome Treatment
1 44 YR Female Required Intervention EXCIMER LASER SN (B)(6).