International safety notice
General names: (1) Single-use Class II treatment kit, (2) Single-use intraocular illumination probe, (3) Vitrectomy uniform Tocuta Handpiece, (4) Single Use Ophthalmic Trocars Sales name: (1)Acurus vitreous surgery pack (2)Alcon Disposable Illuminator (3)UNITY Vitreous Probe (4)UNITY Entry System
Japan / PMDA Recalls · JPN · Aug 25, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General names: (1) Single-use Class II treatment kit, (2) Single-use intraocular illumination probe, (3) Vitrectomy uniform Tocuta Handpiece, (4) Single Use Ophthalmic Trocars Sales name: (1)Acurus vitreous surgery pack (2)Alcon Disposable Illuminator (3)UNITY Vitreous Probe (4)UNITY Entry System |
| Manufacturer | Japan Alcon Co., Ltd. |
| Models | 17E33N, 8065753179, 17C6U5, 8065000250, 8065000467, 8065751577, 17CP3U, 8065000356, 17E77V, 17C2RY, 8065000468, 179MCD and 3 more |
| Date | Aug 25, 2025 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1