International safety notice
It was discovered that the product was manufactured with a different amount from the amount stated on the designated controlled medical device manufacturing and sales certificate. Ta. Therefore, we have decided to recall the lot.
Japan / PMDA Recalls · JPN · Mar 14, 2023
Key facts
| Title | It was discovered that the product was manufactured with a different amount from the amount stated on the designated controlled medical device manufacturing and sales certificate. Ta. Therefore, we have decided to recall the lot. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Manufacturer | Matsukaze Co., Ltd. |
| Models | 032060, 082162, 072263, 112061 |
| Date | Mar 14, 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