Device recall
Z-0900-2011: Horizon Cardiology ECG Management This is a software application designed for…
FDA device recall · Class II · McKesson Provider Technologies - Medical Imaging Group
Key facts
| Recall number (Z-number) | Z-0900-2011 |
|---|---|
| Recall event | 57436 |
| Product | Horizon Cardiology ECG Management This is a software application designed for use in various hospital departments to import, display, store, analyze, distribute, and process ECG procedures from resting ECG devices. It is also intended to provide analysis or reanalysis or testings ECGs and to provide… |
| Product code | DQK |
| Recalling firm | McKesson Provider Technologies - Medical Imaging Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 17, 2012 |
| FEI number | 3005157178 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database