# FDA recall Z-1156-2026

> **Philips North America** · Class II · device recall initiated 2025-12-22.

## Product

Patient Information Center iX;  Software Version Number: 4.5.0

## Reason for recall

A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.

## Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Brazil, Canada, Czech Republic, Dominican Rep, Finland, France, Germany, Greece, Hungary, India, Italy, Japan, Jordan, Netherlands, Norway, Poland, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom, Utd.Arab.Emir.

## Key facts

- **Recall number:** Z-1156-2026
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-22
- **Report date:** 2026-01-28

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1156-2026

## Citation

> AI Analytics. FDA recall Z-1156-2026. Retrieved 2026-07-29 from https://api.ai-analytics.org/recall/Z-1156-2026. Source: US FDA. Licensed CC0.

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