International safety notice
General name: Blood type analysis device Brand name: Fully automatic blood transfusion testing device for cards IH-500
Japan / PMDA Recalls · JPN · Oct 11, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Blood type analysis device Brand name: Fully automatic blood transfusion testing device for cards IH-500 |
| Manufacturer | Bio-Rad Laboratories Co., Ltd. |
| Models | 0500499, 0501665, 0500670, 0400229, 0502133, 0500755, 0500245, 0500697, 0501563, 0400230, 0500821, 0501764 and 161 more |
| Date | Oct 11, 2022 |
| 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