International safety notice
Products manufactured before October 2019 due to a defective pressure sensor in the control board (CR board) installed in the device. We have noticed an increase in the number of problems where the front panel lights go out. We decided to collect it as an elephant.
Japan / PMDA Recalls · JPN · Apr 19, 2024
Key facts
| Title | Products manufactured before October 2019 due to a defective pressure sensor in the control board (CR board) installed in the device. We have noticed an increase in the number of problems where the front panel lights go out. We decided to collect it as an elephant. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Laparoscopic gas pneumoperitoneum device Brand name: High-speed pneumoperitoneum device UHI-4 |
| Manufacturer | Olympus Medical Systems Co., Ltd. |
| Models | 7210590, 7311705, 7741205, 7741578, 7434124, 7536504, 7322513, 7210023, 7946198, 7322290, 7741289, 7945097 and 2902 more |
| Date | Apr 19, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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