International safety notice
General name: Blood type analysis device Brand name: Fully automatic blood transfusion testing device Erytra Eflexis
Japan / PMDA Recalls · JPN · Aug 29, 2024
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Blood type analysis device Brand name: Fully automatic blood transfusion testing device Erytra Eflexis |
| Manufacturer | Kainos Co., Ltd. |
| Models | 511‐0000698, 511‐0001855, 511‐0001606, 511‐0001221, 511‐0001071, 511‐0001126, 511‐0001692, 511‐0000660, 511‐0000604, 511‐0001599, 511‐0000823, 511‐0001522 and 57 more |
| Date | Aug 29, 2024 |
| 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