Device recall
Z-2247-2011: Philips Microstream Model M1923A FILTERLINE H SET INF/NEO 25UN PHILIPS These…
FDA device recall · Class I · Philips Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-2247-2011 |
|---|---|
| Recall event | 58471 |
| Product | Philips Microstream Model M1923A FILTERLINE H SET INF/NEO 25UN PHILIPS These products are used with Philips Monitors for the measurement of endtidal CO2 in infants and neonates. They provide a means to transport samples of patient respiratory gases from the patient's airway to the Microstream… |
| Product code | CCK |
| Recalling firm | Philips Healthcare Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 14, 2013 |
| 510(k) numbers | K980327 |
| FEI number | 1218950 |
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