# FDA recall Z-1033-2026

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

## Product

Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.

## Reason for recall

It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1033-2026
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-12
- **Report date:** 2026-01-14

- **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-1033-2026

## Citation

> AI Analytics. FDA recall Z-1033-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1033-2026. Source: US FDA. Licensed CC0.

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