International safety notice
2030360-001|VU360
New Zealand / Medsafe Recalls · NZL · Jul 5, 2019
Key facts
| Title | 2030360-001|VU360 |
|---|---|
| Regulator | New Zealand / Medsafe Recalls |
| Country | NZL |
| Brand | Interpretive multichannel electrocardiograph |
| Manufacturer | GE Medical Systems Information Technologies Inc |
| Models | 2030360-001, VU360 |
| Event type | Safety Notice |
| Action type | Correction |
| Date | Jul 5, 2019 |
| Regulator page | medsafe.govt.nz |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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