Device recall
Z-2203-2008: 740 Series Multiparameter Monitor Software Version 3.0 Model Numbers: 740-1…
FDA device recall · Class II · CAS Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2203-2008 |
|---|---|
| Recall event | 48666 |
| Product | 740 Series Multiparameter Monitor Software Version 3.0 Model Numbers: 740-1, 740M-1, 740-2T, 740M-2T, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS, 740-3NL, 740M-3NL, 740-3NN, and 740M-3NN CAS Medical Systems, Inc., Branford, Connecticut 06405 Indicated for use for… |
| Product code | MHX |
| Recalling firm | CAS Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 5, 2010 |
| 510(k) numbers | K033048 |
| FEI number | 2244861 |
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