International safety notice
General name: Ultra-conductive magnet-type full-body MR device Sales name: (1) Gyroscan Interra 1.5T (2)Interra Achiba 1.5T (3)Achiba 3.0T (4)Achiba 3.0T TX (5) Whole body MR device Intera/Achieva 1.5T (6) Whole body MR device Achieva 3.0T
Japan / PMDA Recalls · JPN · Sep 16, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General name: Ultra-conductive magnet-type full-body MR device Sales name: (1) Gyroscan Interra 1.5T (2)Interra Achiba 1.5T (3)Achiba 3.0T (4)Achiba 3.0T TX (5) Whole body MR device Intera/Achieva 1.5T (6) Whole body MR device Achieva 3.0T |
| Manufacturer | Philips Japan Co., Ltd. |
| Models | 32567, 38187, 39099, 32480, 32597, 32177, 21938, 22148, 20335, 20326, 32975, 33068 and 68 more |
| Date | Sep 16, 2025 |
| 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