International safety notice
It was discovered that a product was being shipped that had a defect in the pre-shipment calibration of the image enhancement function (LCI), so we took measures to correct the problem. We will voluntarily collect the items.
Japan / PMDA Recalls · JPN · May 30, 2022
Key facts
| Title | It was discovered that a product was being shipped that had a defect in the pre-shipment calibration of the image enhancement function (LCI), so we took measures to correct the problem. We will voluntarily collect the items. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: video flexible colonoscope Brand name: (1) Electronic endoscope EC-760XP/L (2) Electronic endoscope EC-760Z-V/M |
| Manufacturer | Fujifilm Co., Ltd. |
| Models | 1C746G033, 1C757G055, 1C746G080, 1C746G041, 1C746G067, 1C757G076, 1C757G002, 1C746G056, 1C757G037, 1C757G022, 1C746G095, 1C757G027 and 171 more |
| Date | May 30, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
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