FDA Adverse Event Injury Summary report: N

VERION REFERENCE UNIT

MDR report key: 4870989 · Received June 26, 2015

Report

Report Number
3010300699-2015-00504
Event Type
Injury
Date Received
June 26, 2015
Date of Event
February 11, 2015
Report Date
July 31, 2015
Manufacturer
WAVELIGHT GMBH (AGPS)
Product Code
HJB
PMA / PMN Number
NA
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

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. ATTEMPTS HAVE BEEN MADE TO OBTAIN ADDITIONAL INFORMATION, AT THIS TIME THE CUSTOMER HAS INDICATED NO ADDITIONAL INFORMATION WILL BE PROVIDED. (B)(4).

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION PROVIDED: NO TECHNICAL ROOT CAUSE COULD BE DETERMINED. CONTRIBUTING FACTORS FOR REPORTED ISSUE COULD BE A POOR DIAGNOSTIC IMAGE, USE OF A NON OPTIMIZED FORMULA DURING PLANNING, OR INCORRECT PATIENT DATA ENTRY. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).

Description of Event or Problem · 1

A NURSE REPORTED A CASE OF A BILATERAL TORIC INTRAOCULAR LENS EXPLANT, AND INDICATED A DIAGNOSTIC CALCULATION ERROR CREATED AN OVER-CORRECTED REFRACTIVE OUT-COME. PATIENT NOTED VISION WAS BLURRED. UPON ADDITIONAL FOLLOW UP, THE REPORTER WAS UNWILLING TO PROVIDE ANY ADDITIONAL INFORMATION. THERE ARE TWO RELATED REPORTS FOR THIS PATIENT. THIS REPORT ADDRESSES THE PATIENT'S RIGHT EYE, AND ANOTHER MANUFACTURER REPORT WILL BE FILED FOR THE FELLOW EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
416595 VERION REFERENCE UNIT KERATOMETER, PUPILLOMETER HJB WAVELIGHT GMBH (AGPS) X-RUS ASKU

Patients

Seq Age Sex Outcome Treatment
1 Other| R (B)(4), SP ACRYSOF TORIC IQ