# FDA recall Z-2696-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-06-30.

## Product

IntelliVue MX800 patient monitor, model no. 865240

## Reason for recall

Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.

## Distribution

Domestic distribution to CA, HI, MA, NY, and UT. International distribution to Costa Rica, Ireland, Lebanon, and Poland.

## Key facts

- **Recall number:** Z-2696-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-30
- **Report date:** 2020-07-29
- **Termination date:** 2024-01-25

- **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-2696-2020

## Citation

> AI Analytics. FDA recall Z-2696-2020. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-2696-2020. Source: US FDA. Licensed CC0.

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