Device recall
Z-2121-2014: Horizon Medical Imaging It is a medical image and information management…
FDA device recall · Class II · Mckesson Medical Immaging
Key facts
| Recall number (Z-number) | Z-2121-2014 |
|---|---|
| Recall event | 68799 |
| Product | Horizon Medical Imaging It 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 various medical imaging systems. |
| Product code | LLZ |
| Recalling firm | Mckesson Medical Immaging |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2017 |
| 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