INTRAOCULAR LENS
This device is manufactured by ALCON LABORATORIES, ALCON LABORATORIES IRELAND, ALCON MANUFACTURING / HUNTINGTON, ALCON RESEARCH, ALCON RESEARCH - HUNTINGTON.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Visual Impairment | 2 | Patient |
2024 | Insufficient Information | 3 | Patient |
2024 | Blurred Vision | 1 | Patient |
2024 | Material Split, Cut or Torn | 1 | Device |
2024 | Failure to Advance | 1 | Device |
2024 | Device Dislodged or Dislocated | 1 | Device |
2024 | Device Damaged by Another Device | 1 | Device |
2024 | Defective Device | 3 | Device |
2024 | Break | 2 | Device |
2023 | Vitreous Detachment | 1 | Patient |
2023 | Visual Impairment | 3 | Patient |
2023 | Visual Disturbances | 3 | Patient |
2023 | Insufficient Information | 6 | Patient |
2023 | Blurred Vision | 3 | Patient |
2023 | Appropriate Term / Code Not Available | 1 | Patient |
2023 | Unintended Ejection | 1 | Device |
2023 | Scratched Material | 2 | Device |
2023 | Material Opacification | 1 | Device |
2023 | Device Markings/Labelling Problem | 1 | Device |
2023 | Device Dislodged or Dislocated | 3 | Device |
2023 | Defective Device | 2 | Device |
2023 | Break | 1 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
2022 | Scratched Material | 2 | Device |
2022 | Material Split, Cut or Torn | 1 | Device |
2022 | Material Discolored | 1 | Device |
2022 | Failure to Align | 1 | Device |
2022 | Device Dislodged or Dislocated | 1 | Device |
2022 | Device Damaged by Another Device | 1 | Device |
2022 | Device Contamination with Chemical or Other Material | 3 | Device |
2022 | Defective Device | 2 | Device |
2022 | Crack | 1 | Device |
2022 | Appropriate Term/Code Not Available | 2 | Device |