International safety notice
General name: Superconducting magnet-type whole-body MR device Brand name: Whole body MR device Prodiva 1.5T
Japan / PMDA Recalls · JPN · Oct 29, 2021
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Superconducting magnet-type whole-body MR device Brand name: Whole body MR device Prodiva 1.5T |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 82448, 83237, 83242, 83202, 82382 |
| Date | Oct 29, 2021 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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