International safety notice
We found that there was a processing defect in the process of manufacturing this product, in which the handle is connected to the main body. Ta. As it became clear that this was the case, we decided to voluntarily recall the product.
Japan / PMDA Recalls · JPN · Dec 18, 2023
Key facts
| Title | We found that there was a processing defect in the process of manufacturing this product, in which the handle is connected to the main body. Ta. As it became clear that this was the case, we decided to voluntarily recall the product. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | General name: Instruments for spine surgery Brand name: Spinal surgery instruments |
| Manufacturer | Tanaka Medical Instruments Manufacturing Co., Ltd. |
| Models | 22AA01, 23AA02×1, 23AA01×4, 23AA02, 22AA01×5, 23AA01 |
| Date | Dec 18, 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