STAAR ICL CALCULATION SOFTWARE
Report
- Report Number
- 2023826-2026-00743
- 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
- TX, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
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 APRIL 13 AND APRIL 16, 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).
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 PRIOR TO IMPLANTATION, AND THE LENS IS EXPECTED TO BE IMPLANTED USING THE CORRECT ORIENTATION DIAGRAM. NO PATIENT INJURY OR ADVERSE EVENT HAS BEEN REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 385924 | STAAR ICL CALCULATION SOFTWARE | ICL CALCULATION SOFTWARE | MTA | STAAR SURGICAL COMPANY | N/A | N/A | 00840311346288 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |