International safety notice
For certain lots of covered products, the purpose of attaching a reference frame to a patient for image navigation surgery Therefore, when this product is percutaneously placed in the pelvis, the cross pin tap cap cannot be attached to the cross pin part of this product. Alternatively, it has been found that it may be difficult to remove the tap cap from this product when it is placed in the pelvis. Ta.
Japan / PMDA Recalls · JPN · Dec 12, 2023
Key facts
| Title | For certain lots of covered products, the purpose of attaching a reference frame to a patient for image navigation surgery Therefore, when this product is percutaneously placed in the pelvis, the cross pin tap cap cannot be attached to the cross pin part of this product. Alternatively, it has been found that it may be difficult to remove the tap cap from this product when it is placed in the pelvis. Ta. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Single Use Bone Surgery Instrument Brand name: Sterilized pin |
| Manufacturer | Japan Medtronic Co., Ltd. |
| Models | 2022030438, 2023041136, 9733236 |
| Date | Dec 12, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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