International safety notice
We have determined that a portion of the product may fall into the patient's body, so we have decided to carry out a voluntary recall. did.
Japan / PMDA Recalls · JPN · Sep 20, 2023
Key facts
| Title | We have determined that a portion of the product may fall into the patient's body, so we have decided to carry out a voluntary recall. did. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Single-use endoscopic non-active treatment device for natural opening Brand name: PENTAX Medical cold snare for endoscope VDK-CS |
| Manufacturer | HOYA Co., Ltd. |
| Models | 2023040701CS, VDK-CS-23-230-10-C3P |
| Date | Sep 20, 2023 |
| 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