International safety notice
General names: (1) Indenter for single-use organ fixation (2) Indenter for single-use organ fixation (3) Indenter for single-use organ fixation Sales name: (1)ACROBAT-i stabilizer (2)ACROBAT-i Positioner (3)Acrobatic SUV
Japan / PMDA Recalls · JPN · Mar 4, 2025
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General names: (1) Indenter for single-use organ fixation (2) Indenter for single-use organ fixation (3) Indenter for single-use organ fixation Sales name: (1)ACROBAT-i stabilizer (2)ACROBAT-i Positioner (3)Acrobatic SUV |
| Manufacturer | Getinge Group Japan Co., Ltd. |
| Models | 3000351774, 3000321412, 3000311731, 3000338107, 3000341430, OM-10000Z, 3000361797, 3000336377, 3000314838, 3000394893, OM-9000Z, XP-5000Z and 14 more |
| Date | Mar 4, 2025 |
| 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