# FDA recall Z-1827-2024

> **Philips North America Llc** · Class II · device recall initiated 2024-04-19.

## Product

Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.

## Reason for recall

Event Catalog information does not save when copied and transferred from one unit to another.

## Distribution

Worldwide - US Nationwide distribution in the states of CA, FL, GA, IA, MA, MI, MN, MO, NJ, NM, NY, OH, PA, TN, TX, WA, WV, & DC. The countries of AE, AT, AU, BE, BR, CA, CH, CZ, DE, DK, ES, FI, FR, GB, IE, IL, IN, IT, JP, KR, LT, NL, NO, OM, PL, PT, RO, SE, SG, SK, TH, & ZA.

## Key facts

- **Recall number:** Z-1827-2024
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-19
- **Report date:** 2024-05-22

- **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-1827-2024

## Citation

> AI Analytics. FDA recall Z-1827-2024. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1827-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*