International safety notice
We have received a report from the manufacturer that a component (tube) that has not gone through the appropriate manufacturing process may have been used in the product. did.
Japan / PMDA Recalls · JPN · Jun 24, 2024
Key facts
| Title | We have received a report from the manufacturer that a component (tube) that has not gone through the appropriate manufacturing process may have been used in the product. did. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Needleless contrast medium infusion set Sales name: RAQUOS disposable kit |
| Manufacturer | Dbx Co., Ltd. |
| Models | 2310003, 2312016, 2402015, 2310013, 2402017, 2402016, 2404003, 2404004, 2312009, 2311005, 2402003, 2402004 and 3 more |
| Date | Jun 24, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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