International safety notice
The affected product (sales name: Endopath Surgery Probe, product number: EPS06) has been issued by an overseas manufacturer. The package contains a product (same brand name, product number: EPS01) that is different from the product number (EPS06) written on the product box and sterile packaging. I received notification that there is a possibility of
Japan / PMDA Recalls · JPN · May 10, 2022
Key facts
| Title | The affected product (sales name: Endopath Surgery Probe, product number: EPS06) has been issued by an overseas manufacturer. The package contains a product (same brand name, product number: EPS01) that is different from the product number (EPS06) written on the product box and sterile packaging. I received notification that there is a possibility of |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Endoscopic irrigation and aspiration probe Brand name: Endopath Surgery Probe |
| Manufacturer | Johnson & Johnson Co., Ltd. |
| Models | U94Y4V, EPS06 |
| Date | May 10, 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