International safety notice
This product is an internal fixation plate used for maxillary and maxillary bone fixation, surgical correction, mandibular reconstruction, and treatment of jaw deformity. Rate. Upon checking the domestic inventory, it was discovered that the same problem had occurred in the products in the affected lot. With an emphasis on patient safety, we have decided to voluntarily recall the affected products.
Japan / PMDA Recalls · JPN · Mar 24, 2023
Key facts
| Title | This product is an internal fixation plate used for maxillary and maxillary bone fixation, surgical correction, mandibular reconstruction, and treatment of jaw deformity. Rate. Upon checking the domestic inventory, it was discovered that the same problem had occurred in the products in the affected lot. With an emphasis on patient safety, we have decided to voluntarily recall the affected products. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Internal fixation plate Sales name: MOJ System |
| Manufacturer | Johnson & Johnson Co., Ltd. |
| Models | 1446P77, 04-511-966S |
| Date | Mar 24, 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