Device recall
Z-1771-2019: Philips Patient Information Center iX configured with a regional setting which…
FDA device recall · Class III · Philips North America, LLC
Key facts
| Recall number (Z-number) | Z-1771-2019 |
|---|---|
| Recall event | 82914 |
| Product | Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Information Center iX B.01 (or later); 866390 Patient Information Center iX B.01 upgrade (or later) Product Usage: The intended use of the Information Center Software… |
| Product code | MHX |
| Recalling firm | Philips North America, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 22, 2024 |
| 510(k) numbers | K153702 |
| 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