International safety notice
The product was recalled because it was confirmed that the piping inside the product came off due to vibration during transportation and use, making suction impossible. I decided to do so.
Japan / PMDA Recalls · JPN · Jan 27, 2022
Key facts
| Title | The product was recalled because it was confirmed that the piping inside the product came off due to vibration during transportation and use, making suction impossible. I decided to do so. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Electric portable suction device Brand name: (1) Tabletop suction device BM-1200W-2 (2) 3 Power Suction Unit 3WAY-1200W-2 |
| Manufacturer | Blue Cross Co., Ltd. |
| Models | 2165020102, 2165020123, ３ＷＡＹ‐１２００Ｗ‐２, 2165040112, 2165020096, 2165020001, 2165040001, 2165040005, ＢＭ‐１２００Ｗ‐２, 2165040054, 2165040115, 2165040056 and 4 more |
| Date | Jan 27, 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