International safety notice
General name: Dry clinical chemistry analysis device Brand name: Lumira measuring equipment
Japan / PMDA Recalls · JPN · Nov 15, 2023
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Dry clinical chemistry analysis device Brand name: Lumira measuring equipment |
| Manufacturer | Lumira Diagnostics Japan Co., Ltd. |
| Models | 30874-21-13-31055, 30874-21-17-35326, 30874-22-12-60673, 30874-22-13-61408, 30874-22-18-63399, 30874-22-13-61365, 30874-22-41-67992, 30874-22-08-57964, 30874-21-13-31027, 30874, 22-08-57970, 30874-22-1 and 3 more |
| Date | Nov 15, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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