International safety notice
We received a report from a medical facility that anti-cancer drugs may have been administered at a higher flow rate than the set flow rate. Ta. This may have occurred because the problem could not be blocked and there was no abnormality detection function to detect it. and update the software.
Japan / PMDA Recalls · JPN · Oct 11, 2022
Key facts
| Title | We received a report from a medical facility that anti-cancer drugs may have been administered at a higher flow rate than the set flow rate. Ta. This may have occurred because the problem could not be blocked and there was no abnormality detection function to detect it. and update the software. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Pharmaceutical Infusion Controller Brand name: Infusion controller SEEVOL |
| Manufacturer | Murata Manufacturing Co., Ltd. |
| Models | 10017, 10036, 10050, 10006, 10073, 10015, 10065, 10067, 10053, 10025 |
| Date | Oct 11, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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