International safety notice
We received information from a medical institution that ``a product was contained in an unsealed individual package.'' When we checked the unshipped products, we found that some products had defective seals. Subsequent investigation results revealed similar sealing defects in products manufactured using a specific lot of packaging material. Ta. We have decided to recall 4 lots of affected products.
Japan / PMDA Recalls · JPN · Oct 7, 2022
Key facts
| Title | We received information from a medical institution that ``a product was contained in an unsealed individual package.'' When we checked the unshipped products, we found that some products had defective seals. Subsequent investigation results revealed similar sealing defects in products manufactured using a specific lot of packaging material. Ta. We have decided to recall 4 lots of affected products. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Single-use scalpel Sales name: Feather disposable scalpel |
| Manufacturer | Feather Safety Razor Co., Ltd. |
| Models | 22070741, 22070621, 22070704, 22070657, No.11 |
| Date | Oct 7, 2022 |
| 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