International safety notice
General name: Automatic dyeing device Sales name: Ventana HE 600
Japan / PMDA Recalls · JPN · Jul 22, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Automatic dyeing device Sales name: Ventana HE 600 |
| Manufacturer | Roche Diagnostics Co., Ltd. |
| Models | 6000115, 6000180, 6000392, 000918, 6000667, 6000806, 6000315, 6000787, 6000447, 6000414, 6000028, 6000429 and 30 more |
| Date | Jul 22, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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