International safety notice
We have received complaints both in Japan and overseas that the catalog number on the label affixed to the package is different from the packaged product. We have received it. 13203042S (AO type connection shape) and 13203042S (AO type connection shape), and as a result, the product is displayed as 13203045S. It has been discovered that the product may contain 13203042S. We have decided to carry out a voluntary recall.
Japan / PMDA Recalls · JPN · Nov 15, 2021
Key facts
| Title | We have received complaints both in Japan and overseas that the catalog number on the label affixed to the package is different from the packaged product. We have received it. 13203042S (AO type connection shape) and 13203042S (AO type connection shape), and as a result, the product is displayed as 13203045S. It has been discovered that the product may contain 13203042S. We have decided to carry out a voluntary recall. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Single-use bone surgery instrument Brand name: Single-use surgical instrument K for trauma (sterilized) |
| Manufacturer | Japan Striker Co., Ltd. |
| Models | K02F0CA, 13203045S |
| Date | Nov 15, 2021 |
| 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