Device recall
Z-1266-2010: 100-120V Capnogard 1265, Respironics/Philips product. Intended to be used for…
FDA device recall · Class II · Philips Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-1266-2010 |
|---|---|
| Recall event | 53869 |
| Product | 100-120V Capnogard 1265, Respironics/Philips product. Intended to be used for monitoring end tidal CO2 and respiration rate in all critical monitoring environments. |
| Product code | CCK |
| Recalling firm | Philips Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 8, 2016 |
| 510(k) numbers | K910019 |
| FEI number | 1218950 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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