International safety notice
General name: Superconducting magnet-type whole-body MR device Sales name: (1) MAGNETOM Aela (2) MAGNETOM Avant (3) MAGNETOM Amira (4) MAGNETOM Vida (5) MAGNETOM Skyla (6) MAGNETOM Spectra (7) MAGNETOM Sempra (8) MAGNETOM Sora (9) MAGNETOM Free Max/Free Star (10) MAGNETOM Prisma
Japan / PMDA Recalls · JPN · Oct 24, 2023
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Superconducting magnet-type whole-body MR device Sales name: (1) MAGNETOM Aela (2) MAGNETOM Avant (3) MAGNETOM Amira (4) MAGNETOM Vida (5) MAGNETOM Skyla (6) MAGNETOM Spectra (7) MAGNETOM Sempra (8) MAGNETOM Sora (9) MAGNETOM Free Max/Free Star (10) MAGNETOM Prisma |
| Manufacturer | Siemens Healthcare Co., Ltd. |
| Models | 180013, 45874, 200062, 66083, 69642, 52305, 145368, 193625, 177659, 45781, 179450, 193567 and 961 more |
| Date | Oct 24, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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