International safety notice
The product in question does not meet our standards for the amount of force required to open and close the grip. We are conducting a voluntary recall as we have discovered that this is a possibility.
Japan / PMDA Recalls · JPN · May 24, 2022
Key facts
| Title | The product in question does not meet our standards for the amount of force required to open and close the grip. We are conducting a voluntary recall as we have discovered that this is a possibility. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | (1) Common name: Single-use endoscopic stone removal forceps Brand name: Disposable grasping forceps for bile ducts (2) Common name: ureteral stone removal tubes and catheters Brand name: Disposable grasping forceps for ureter |
| Manufacturer | Olympus Medical Systems Co., Ltd. |
| Models | FG-55D, FG-51D |
| Date | May 24, 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