Device recall
Z-0710-2008: Horizon Cardiology Hemo Monitoring System;Horizon Cardiology Hemo External…
FDA device recall · Class II · McKesson Provider Technologies
Key facts
| Recall number (Z-number) | Z-0710-2008 |
|---|---|
| Recall event | 46276 |
| Product | Horizon Cardiology Hemo Monitoring System;Horizon Cardiology Hemo External Control Unit;~100 - 230 VAC 50-50 Hz, Medcon Telemedicine Technology LTD.,Tel Aviv, 697190, Israel. |
| Product code | DQK |
| Recalling firm | McKesson Provider Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 28, 2008 |
| 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