International safety notice
Regarding lot 1D01 of the product, it was discovered that there was a discrepancy in the sterility certification with the approval certificate, so we decided to voluntarily recall the product. did.
Japan / PMDA Recalls · JPN · Oct 25, 2023
Key facts
| Title | Regarding lot 1D01 of the product, it was discovered that there was a discrepancy in the sterility certification with the approval certificate, so we decided to voluntarily recall the product. did. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Submucosal injection material for endoscopy Brand name: Riftal K |
| Manufacturer | Kaigen Pharma Co., Ltd. |
| Date | Oct 25, 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