Device recall
Z-1873-2009: Welch Allyn Vital Sign Monitor 5300 Series/Class II. (VSM 300). The VSM300 can…
FDA device recall · Class II · Welch Allyn Protocol, Inc
Key facts
| Recall number (Z-number) | Z-1873-2009 |
|---|---|
| Recall event | 52721 |
| Product | Welch Allyn Vital Sign Monitor 5300 Series/Class II. (VSM 300). The VSM300 can monitor systolic and diastolic noninvasive blood pressure (NIBP), pulse rate, and mean arterial pressure (MAP). Units configured with the appropriate options can also simultaneously monitor temperature and noninvasive… |
| Product code | MWI |
| Recalling firm | Welch Allyn Protocol, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 10, 2011 |
| 510(k) numbers | K053027, K063419 |
| FEI number | 3023750 |
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