International safety notice
Software del Centricity PACS-IW V3.7.x V3.7.x a 3.7.3.9 SP3, Centricity PACS-IW con software Universal Viewer V5.0 SPx con base PACS-IW y Centricity Universal Viewer con software de base PACS-IW V6.0 SP0 a 6.0 SP7.1.
Spain / AEMPS · ESP · Oct 11, 2023
Key facts
| Title | Software del Centricity PACS-IW V3.7.x V3.7.x a 3.7.3.9 SP3, Centricity PACS-IW con software Universal Viewer V5.0 SPx con base PACS-IW y Centricity Universal Viewer con software de base PACS-IW V6.0 SP0 a 6.0 SP7.1. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Software del Centricity PACS-IW V3.7.x V3.7.x a 3.7.3.9 SP3, Centricity PACS-IW con software Universal Viewer V5.0 SPx con base PACS-IW y Centricity Universal Viewer con software de base PACS-IW V6.0 SP0 a 6.0 SP7.1. |
| Manufacturer | GE Medical Systems, LLC, EEUU. |
| Models | 2023-471, SP7.1, 28022, 28023, 3.7.3.9, V3.7.X, RECALL.85470, ALERTA2023-471, 91.822.52.89, 18446744073710815816, 85470, 35-37 and 2 more |
| Event type | Safety Notice |
| Date | Oct 11, 2023 |
At a glance
- No Recall
- Yes 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