device · product 1 of 1
Philips IntelliVue Information Center iX (release A.00, A.01, and A.02) are impacted by this issue: 866023 IntelliVue Info Center iX 866024 PIIC iX Upgrade 866117 PIIC Classic Upgrade The intended use of the Information Center Software is to display physiologic waves, parameters, and trends, format data for strip chart recordings and printed reports, and provide the secondary annunciation of alarms from other networked medical devices at a centralized location. An additional intended use of the Information Center Software is to provide primary annunciation of alarms and configuration and control access for networked telemetry monitors.
- Recall number
- Z-0374-2016
- Initiated
- December 19, 2014
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Philips Medical Systems, Inc.
- Quantity
- 10,013 units
App-derived interpretation
Unknown
Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled without visual notification
Official device-enrichment evidence · Sourced
Software Design Change
Inspect official wording and provenance
Reason for recall
Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled without visual notification
Code information
Software systems Revision A.02.05 or lower
Distribution pattern
Worldwide Distribution: US (nationwide) and countries: AUSTRALIA, AUSTRIA, BELGIUM, BULGARIA, CANADA, DENMARK, ESTONIA, FINLAND, FRANCE, GERMANY, HUNGARY, ICELAND, INDIA, IRAQ, IRELAND, ISRAEL, ITALY, JAPAN, LUXEMBOURG, MOROCCO, NETHERLANDS, NEW ZEALAND, NIGERIA, NORWAY, POLAND, PORTUGAL, QATAR, ROMANIA, RUSSIAN FEDERATION, SINGAPORE, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, UNITED ARAB EMIRATES, and UNITED KINGDOM.