# FDA recall Z-1315-2018

> **Philips Electronics North  America Corporation** · Class II · device recall initiated 2017-11-17.

## Product

IntelliVue X3 Patient Monitor.

## Reason for recall

The NBP measurement of Intellivue X3 Patient Monitor shows intermittently only mean values instead of the diastolic and systolic blood pressure values. This is caused by a falsely detected NBP cuff, which is leading to wrong internal NBP setting. Furthermore, occasionally the Monitor shows the  Check Touch Input  message and the monitor is inoperable with the touch interface.

## Distribution

48 Foreign Accounts

## Key facts

- **Recall number:** Z-1315-2018
- **Recalling firm:** Philips Electronics North  America Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-17
- **Report date:** 2018-04-18
- **Termination date:** 2020-09-16

- **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-1315-2018

## Citation

> AI Analytics. FDA recall Z-1315-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1315-2018. Source: US FDA. Licensed CC0.

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