International safety notice
The "single-use ophthalmic knife" manufactured by Feather Safety Razor Co., Ltd. is included in the kit product manufactured by our company. In "Micro Feather Plastic Handle", "the blade fixed to the handle (handle) may change over time after manufacturing. "This may reduce the strength of the blade's fixation, and in some cases it may fall off the handle," says the manufacturer, Feather. We received a report from Safety Razor Co., Ltd. At the same time, we have received notification from Feather Safety Razor Co., Ltd., the manufacturer and distributor, that they will be voluntarily recalling the product. We have decided to voluntarily recall our products that make up the item.
Japan / PMDA Recalls · JPN · Aug 30, 2023
Key facts
| Title | The "single-use ophthalmic knife" manufactured by Feather Safety Razor Co., Ltd. is included in the kit product manufactured by our company. In "Micro Feather Plastic Handle", "the blade fixed to the handle (handle) may change over time after manufacturing. "This may reduce the strength of the blade's fixation, and in some cases it may fall off the handle," says the manufacturer, Feather. We received a report from Safety Razor Co., Ltd. At the same time, we have received notification from Feather Safety Razor Co., Ltd., the manufacturer and distributor, that they will be voluntarily recalling the product. We have decided to voluntarily recall our products that make up the item. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Single Use Class III Treatment Kit Sales name: Ophthalmology kit |
| Manufacturer | Japan Medical Products Co., Ltd. |
| Models | 7317800, HP-E1262, 448731, 449151, 449571, HP-E1182, 448471, 7401000, 451211, 450011, 448481, 448171 and 14 more |
| Date | Aug 30, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
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