Device recall
Z-0042-2015: McKesson Cardiology" Hemo intended for complete physiological/hemodynamic…
FDA device recall · Class II · Mckesson Information Solutions LLC
Key facts
| Recall number (Z-number) | Z-0042-2015 |
|---|---|
| Recall event | 69377 |
| Product | McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment. |
| Product code | MWI |
| Recalling firm | Mckesson Information Solutions LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 18, 2016 |
| 510(k) numbers | K131497 |
| FEI number | 3002684279 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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