Drug recall
Philips Patient Information Center iX REF:866389
FDA recall event 99566 · Class II · Philips North America
Key facts
| Event ID | 99566 |
|---|---|
| Recall numbers | Z-3141-2026, Z-3142-2026 |
| Recalling firm | Philips North America |
| Product type | Devices |
| Products | Philips Patient Information Center iX REF:866389, Philips PIC iX Essentials REF:867093 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to software malfunction, patient information system may freeze and become unresponsive. |
| Initiation date | Jul 31, 2026 |
| Report date | Sep 23, 2026 |
| City | Cambridge |
| State | MA |
| Country | United States |
| FEI number | 3006648320 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: