International safety notice
Domestic medical institutions have reported cases of contamination with products of different shapes. However, there is a possibility that similar defects may occur for all products with the product number (376780) shipped to the domestic market. Since we cannot deny this, we have decided to carry out a voluntary recall.
Japan / PMDA Recalls · JPN · Sep 7, 2022
Key facts
| Title | Domestic medical institutions have reported cases of contamination with products of different shapes. However, there is a possibility that similar defects may occur for all products with the product number (376780) shipped to the domestic market. Since we cannot deny this, we have decided to carry out a voluntary recall. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Single-use scalpel Sales name: Beaver Blade |
| Manufacturer | Beaver Visitec International Japan Co., Ltd. |
| Models | 6039837, 376780, 6007681, 6034831, 6015367 |
| Date | Sep 7, 2022 |
| 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