MULTIFOCAL IOLS
This device is manufactured by ABBOTT MEDICAL OPTICS.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Visual Impairment | 1 | Patient |
| 2024 | Visual Disturbances | 4 | Patient |
| 2024 | Posterior Capsule Opacification | 1 | Patient |
| 2024 | Halo | 2 | Patient |
| 2024 | Eye Pain | 2 | Patient |
| 2024 | Eye Injury | 1 | Patient |
| 2024 | Blurred Vision | 6 | Patient |
| 2024 | Break | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 5 | Device |
| 2023 | Visual Impairment | 1 | Patient |
| 2023 | Visual Disturbances | 1 | Patient |
| 2023 | Halo | 1 | Patient |
| 2023 | Corneal Edema | 1 | Patient |
| 2023 | Appropriate Term / Code Not Available | 2 | Patient |
| 2023 | Mechanical Problem | 1 | Device |
| 2023 | Material Opacification | 1 | Device |
| 2023 | Device Dislodged or Dislocated | 1 | Device |
| 2023 | Break | 1 | Device |
| 2023 | Appropriate Term/Code Not Available | 1 | Device |
| 2023 | Application Program Problem: Dose Calculation Error | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2022 | Visual Impairment | 1 | Patient |
| 2022 | Scratched Material | 1 | Device |
| 2022 | Material Opacification | 2 | Device |
| 2022 | Manufacturing, Packaging or Shipping Problem | 1 | Device |
| 2022 | Delivered as Unsterile Product | 1 | Device |
| 2022 | Break | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
| 2020 | Product Quality Problem | 1 | Device |
| 2020 | Adverse Event Without Identified Device or Use Problem | 14 | Device |