FDA Device recall Z-3141-2026
Philips Patient Information Center iX REF:866389
- FDA Device
- Class II
- ongoing
- Published 2026-09-23
On 2026-09-23 the FDA classified a Class II recall of Philips Patient Information Center iX REF:866389 by Philips North America, citing due to software malfunction, patient information system may freeze and become unresponsive.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3141-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-31 |
| Published | 2026-09-23 |
| Last updated | 2026-09-29 05:30 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Philips Patient Information Center iX REF:866389
Reason
Due to software malfunction, patient information system may freeze and become unresponsive.
Identifiers
| code_info | All PIC iX software versions 4.0-4.5/UDI: (01)00884838127067 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-29 05:30 UTC. Current status: ongoing.
Other recalls by Philips North America
- Ingenia 3.0T and 3.0T CX
FDA Device · Class II · 2026-10-07 · Philips North America - MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - SmartPath to MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - Upgrade to MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - Upgrade dStream
FDA Device · Class II · 2026-10-07 · Philips North America
All Philips North America recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3141-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.