International safety notice
General name: Single-use endoscope needle Sales name: Primeject
Japan / PMDA Recalls · JPN · May 15, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Single-use endoscope needle Sales name: Primeject |
| Manufacturer | Lake R&D Inc. |
| Models | 24704045, 23701045, 24706044, 23003046, M00504560, M00504570, 24703045, 24707044, 23605045, 24708044, 24A13045, 23702045 and 2 more |
| Date | May 15, 2025 |
| 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