International safety notice
Common name: aortic cannula Sales name: DLP Myocardial Protective Fluid Injection Cannula
Japan / PMDA Recalls · JPN · Feb 6, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: aortic cannula Sales name: DLP Myocardial Protective Fluid Injection Cannula |
| Manufacturer | Japan Medtronic Co., Ltd. |
| Models | 2023031042, 2023041221, 2023020423, 2023100897, 2022020477, 2022050026, 2024010435, 11014, 2024010566, 2022071072, 2023040853, 2024030256 and 77 more |
| Date | Feb 6, 2025 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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