Device recall
Z-2238-2012: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is a…
FDA device recall · Class II · Mckesson Medical Imaging Group
Key facts
| Recall number (Z-number) | Z-2238-2012 |
|---|---|
| Recall event | 62567 |
| Product | Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is a medical image and information management application that is intended to receive, transmit store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from… |
| Product code | LLZ |
| Recalling firm | Mckesson Medical Imaging Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 12, 2013 |
| 510(k) numbers | K043146 |
| FEI number | 3003757840 |
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