Device recall
Z-0910-2015: McKesson Cardiology ECG Management It is a software application designed to…
FDA device recall · Class II · McKesson Israel Ltd.
Key facts
| Recall number (Z-number) | Z-0910-2015 |
|---|---|
| Recall event | 70144 |
| Product | McKesson Cardiology ECG Management It is a software application designed to import, display, store, analyze, distribute and manage information related to ECG procedures of adult and pediatric patients from external ECG devices. |
| Product code | DQK |
| Recalling firm | McKesson Israel Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 25, 2016 |
| 510(k) numbers | K113515 |
| FEI number | 3007784465 |
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