International safety notice
It has been confirmed that some products with "Trocar Kits" had damaged sterile packaging. Since the possibility of damage cannot be ruled out, we have decided to carry out a voluntary recall.
Japan / PMDA Recalls · JPN · Feb 22, 2023
Key facts
| Title | It has been confirmed that some products with "Trocar Kits" had damaged sterile packaging. Since the possibility of damage cannot be ruled out, we have decided to carry out a voluntary recall. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Single Use Ophthalmic Surgery Tube Cannula Sales name: Mani Trocar Kit |
| Manufacturer | Manny Co., Ltd. |
| Models | V220013400, V220017100, V220012500, V220018001, V220000702, V220000700, V210029304, V210024500, V220016002, V210027302, V210026200, V210026201 and 55 more |
| Date | Feb 22, 2023 |
| 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