FDA Adverse Event Malfunction Summary report: N

STAAR ICL CALCULATION SOFTWARE

MDR report key: 25050994 · Received April 30, 2026

Report

Report Number
2023826-2026-00726
Event Type
Malfunction
Date Received
April 30, 2026
Report Date
April 30, 2026
Manufacturer
STAAR SURGICAL COMPANY
Product Code
MTA
UDI-DI
00840311346288
PMA / PMN Number
P030016/S001
Removal / Correction Number
9614429/04302026/C/001
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

MANUFACTURER NARRATIVE: INVESTIGATION IDENTIFIED A CODING ERROR WITHIN THE STELLA 2.0 PROGRAM SOFTWARE; WHEN A CUSTOMER HAS MULTIPLE TORIC LENS LINE ITEMS IN STELLA (MULTIPLE TORIC LENS RESERVATIONS FOR THE SAME EYE) AND AN IOD IS GENERATED FROM THE PATIENT'S LIST VIEW PAGE, ORDER CONFIRMATION OR SHOPPING CART, THE SYSTEM MAY INCORRECTLY DISPLAY THE SAME PLACEMENT AXIS FOR ALL RESERVED TORIC LENSES INSTEAD OF THE CORRECT PLACEMENT AXIS ASSOCIATED WITH EACH INDIVIDUAL LENS LINE ITEM. ONLY THE IMPLANT ORIENTATION DIAGRAM (IOD) PRINTED USING STELLA 2.0 BETWEEN (B)(6) 2026, AND NOT THE LENS ITSELF, IS AFFECTED BY THIS ISSUE. D2 - THE PRODUCT CODE "MTA" IS ENTERED TO SATISFY MANDATORY FIELD REQUIREMENTS, AS THE DEVICE SOFTWARE IS NOT CURRENTLY CLASSIFIED AND DOES NOT HAVE AN ASSIGNED FDA PRODUCT CODE. G4 PMA/510(K): P030016/S001/A016 CLAIM# (B)(4).

Description of Event or Problem · 0

THE REPORTER INDICATED THAT THE STELLA 2.0 IMPLANT ORIENTATION DIAGRAM (IOD) SOFTWARE GENERATED AN INCORRECT LENS ORIENTATION DIAGRAM DURING LENS SELECTION. THE ISSUE WAS IDENTIFIED AT THE TIME OF LENS ORDERING, PRIOR TO IMPLANTATION; THEREFORE, THERE IS NO KNOWN PATIENT INVOLVEMENT OR ADVERSE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
385684 STAAR ICL CALCULATION SOFTWARE ICL CALCULATION SOFTWARE MTA STAAR SURGICAL COMPANY N/A N/A 00840311346288

Patients

Seq Age Sex Outcome Treatment
1