Device recall
Z-0831-05: Advisor Vital Signs Monitor (model 9200) with Capnography options installed…
FDA device recall · Class III · Smiths Medical PM, Inc.
Key facts
| Recall number (Z-number) | Z-0831-05 |
|---|---|
| Recall event | 31505 |
| Product | Advisor Vital Signs Monitor (model 9200) with Capnography options installed (model 9212S or model 9212A), catalog no. 925674320. |
| Product code | DPS |
| Recalling firm | Smiths Medical PM, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 31, 2006 |
| 510(k) numbers | K010770, K011177 |
| FEI number | 2183502 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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