Device recall
Z-1182-2016: McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9…
FDA device recall · Class II · Mckesson Medical Immaging
Key facts
| Recall number (Z-number) | Z-1182-2016 |
|---|---|
| Recall event | 73452 |
| Product | McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products 12.0 and 12.1.1. |
| Product code | LLZ |
| Recalling firm | Mckesson Medical Immaging |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2018 |
| 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