International safety notice
This product is a specialized infrared-enabled video camera designed for use with endoscopes that converts optical images into electronic video images. This is the device that converts it into The image may be unintentionally reversed if you perform certain operations when using the Luminance Camera Head (Catalog Number: 1688-310-130I). It turned out that it is possible. Although the problem does not occur, as a permanent countermeasure, the software for the 1688 AIM 4K camera console, which is the main unit, We have decided to implement a voluntary recall to update the software to Ver. 4.0.19 or higher.
Japan / PMDA Recalls · JPN · Jun 8, 2022
Key facts
| Title | This product is a specialized infrared-enabled video camera designed for use with endoscopes that converts optical images into electronic video images. This is the device that converts it into The image may be unintentionally reversed if you perform certain operations when using the Luminance Camera Head (Catalog Number: 1688-310-130I). It turned out that it is possible. Although the problem does not occur, as a permanent countermeasure, the software for the 1688 AIM 4K camera console, which is the main unit, We have decided to implement a voluntary recall to update the software to Ver. 4.0.19 or higher. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Endoscopic video camera Sales name: 1688 AIM 4K camera |
| Manufacturer | Japan Striker Co., Ltd. |
| Models | 21A580204, 22B522874, 21K587384, 21I568514, 21E577594, 20I517504, 19G568494, 20A542104, 21B516104, 21A547324, 20A542014, 21D567964 and 266 more |
| Date | Jun 8, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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