Device recall
Z-1974-2010: Horizon Cardiology Hemo Component Schiller Argus Pro PB-1000 Monitor unit. Argus…
FDA device recall · Class II · McKesson Provider Technologies - Medical Imaging Group
Key facts
| Recall number (Z-number) | Z-1974-2010 |
|---|---|
| Recall event | 55598 |
| Product | Horizon Cardiology Hemo Component Schiller Argus Pro PB-1000 Monitor unit. Argus Pro PB 1000 firmware versions 2.41+M NIBP and 2.42.01+M. A programmable diagnostic computer intended for acquiring, digitizing, storing, displaying and reviewing hemodynamic data for use in hospital cardiac… |
| Product code | DQK |
| Recalling firm | McKesson Provider Technologies - Medical Imaging Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 21, 2010 |
| 510(k) numbers | K050561 |
| FEI number | 3005157178 |
At a glance
- 1–9 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