Device recall
Z-2583-2011: Philips SureSigns VM Series Patient Monitors: VM4, VM6, VM 8: Model Part Numbers…
FDA device recall · Class II · Philips Healthcare Inc.
Key facts
| Recall number (Z-number) | Z-2583-2011 |
|---|---|
| Recall event | 59037 |
| Product | Philips SureSigns VM Series Patient Monitors: VM4, VM6, VM 8: Model Part Numbers VM4 863063, 453564024371, 453564021961, 453564024401, 453564021971 VM6 863064, 863065, 453564024421, 453564022001, 453564024441, 453564022041 VM8 863066, 863068, 453564022081, 453564024461, 453564024481 The SureSigns… |
| Product code | MHX |
| Recalling firm | Philips Healthcare Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2013 |
| 510(k) numbers | K101067 |
| FEI number | 1218950 |
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