International safety notice
Applicable product (sales name: BVI cannula (flow-through), product number: FT-12150, lot: SP21J2115) from an overseas manufacturer. 84173), we were informed that adhesive was found in the tube lumen. I decided to mainly collect it.
Japan / PMDA Recalls · JPN · May 13, 2022
Key facts
| Title | Applicable product (sales name: BVI cannula (flow-through), product number: FT-12150, lot: SP21J2115) from an overseas manufacturer. 84173), we were informed that adhesive was found in the tube lumen. I decided to mainly collect it. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Cardiovascular suturing aid Brand name: BVI cannula (flow-through) |
| Manufacturer | Japan ACP Co., Ltd. |
| Models | FT-12150, SP21J211584173 |
| Date | May 13, 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