International safety notice
This product is used for bone fixation after trauma, reconstruction, or osteotomy of the craniomaxillofacial (frontal bone, cheekbone, maxilla, etc.). This time, a different product was found in a package labeled "MatrixMidface Screw 4mm Self-Drilling 4 Pieces". (5mm self-tapping screw) was confirmed to be packaged. I'm here.
Japan / PMDA Recalls · JPN · Nov 20, 2023
Key facts
| Title | This product is used for bone fixation after trauma, reconstruction, or osteotomy of the craniomaxillofacial (frontal bone, cheekbone, maxilla, etc.). This time, a different product was found in a package labeled "MatrixMidface Screw 4mm Self-Drilling 4 Pieces". (5mm self-tapping screw) was confirmed to be packaged. I'm here. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Internal fixation plate Sales name: AO Matrix Midface System |
| Manufacturer | Johnson & Johnson Co., Ltd. |
| Models | 04-503-224-04S |
| Date | Nov 20, 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