# FDA recall Z-0776-2018

> **Philips Electronics North  America Corporation** · Class II · device recall initiated 2018-01-03.

## Product

Intellivue iX Information Center Software - All PIIC iX Surveillance stations including:  866023 IntelliVue Info Center iX A.0  866117 PIIC Classic Upgrade  866389 IntelliVue Info Center iX B.0, C.0  867141 IntelliVue Info Center iX B.0  866025 IntelliVue Server IX A.0  866118 Database Server Upgrade A.0

## Reason for recall

Once a surveillance station is restarted on January 1, 2018 or later, the station will be unable to perform patient discharge and transfer operations. Any subsequent attempt to perform these operations will cause the station to restart, resulting in a short period of loss of monitoring at the Surveillance station during such restart. Until this issue can be corrected, users should avoid intentionally restarting their Surveillance stations in 2018.

## Distribution

Domestic and Foreign

## Key facts

- **Recall number:** Z-0776-2018
- **Recalling firm:** Philips Electronics North  America Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-03
- **Report date:** 2018-03-07
- **Termination date:** 2019-11-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0776-2018

## Citation

> AI Analytics. FDA recall Z-0776-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0776-2018. Source: US FDA. Licensed CC0.

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