International safety notice
On some parts of this device, pressing the front operation panel buttons (power ON/OFF button, option button, shock button) Due to a problem that may not respond depending on the method, a voluntary recall was initiated on December 25, 2006 (2-2438), and corrective action was taken. However, due to information from overseas manufacturers, some devices were excluded from the voluntary recall. It turned out that it was.
Japan / PMDA Recalls · JPN · Jul 13, 2021
Key facts
| Title | On some parts of this device, pressing the front operation panel buttons (power ON/OFF button, option button, shock button) Due to a problem that may not respond depending on the method, a voluntary recall was initiated on December 25, 2006 (2-2438), and corrective action was taken. However, due to information from overseas manufacturers, some devices were excluded from the voluntary recall. It turned out that it was. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 0205142344 |
| Date | Jul 13, 2021 |
| 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