Device recall
Z-1577-2016: Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor…
FDA device recall · Class I · Medtronic
Key facts
| Recall number (Z-number) | Z-1577-2016 |
|---|---|
| Recall event | 73701 |
| Product | Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400, 010520. Battery Pack used with the Capnostream"20 and Capnostream"20p Patient Monitor. The battery pack powers the monitor when AC power is not available or when monitoring is required… |
| Product code | CCK |
| Recalling firm | Medtronic |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 17, 2017 |
| 510(k) numbers | K123690 |
| FEI number | 2936999 |
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