Philips IntellVue Info Center iX 866023 — Class II medical device recall Z-1783-2014
Terminated recall by Philips Healthcare Inc., reported 2014-06-18, distributed nationwide. If a customer creates customized trend scales in the trend review tile and the iX or primary server reboots fo
| Recall number | Z-1783-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2013-03-05 |
| Classified | 2014-06-11 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2017-05-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 899 |
Product
Philips IntellVue Info Center iX 866023; PIIC iX Upgrade 866024; IntellVue Server iX Upgrade 866026; PIIC Classic Upgrade 866117 Patient Physiological Monitor.
Reason for recall
If a customer creates customized trend scales in the trend review tile and the iX or primary server reboots for any reason, the iX(s) will enter a reboot loop. If one iX reboots, the issue will impact only those patients monitored on that device. If the primary server reboots, all patients across all iX devices will be impacted.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1783-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.