Device recall
Z-0178-2008: Capnostream20 Monitor with Masimo Pulse Oximetry Module - Part Number: CS 08659…
FDA device recall · Class II · Oridion Capnography Inc
Key facts
| Recall number (Z-number) | Z-0178-2008 |
|---|---|
| Recall event | 44926 |
| Product | Capnostream20 Monitor with Masimo Pulse Oximetry Module - Part Number: CS 08659 - Oridion Medical |
| Product code | DQA |
| Recalling firm | Oridion Capnography Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 8, 2008 |
| 510(k) numbers | K060065 |
| FEI number | 3006678365 |
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