# FDA recall Z-1767-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-03-05.

## Product

TRx4841A 1.4 GHz IntelliVue Tele TRX, Model Number 862439;  Includes System   Codes 453564007261, 453564007271, 453564007281, 989803196951

## Reason for recall

The ECG signal from patients being monitored using a Philips TRx4841A and TRx4851A Telemetry Transceiver may not be properly analyzed when it is used with a Philips Patient Information Center iX Release C.02.xx or C.03.01. If this occurs, the Information Center will not display a heart rate or generate, display or annunciate any heart rate or arrhythmia alarms.

## Distribution

The products were distributed US nationwide.  Global distribution.

## Key facts

- **Recall number:** Z-1767-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-05
- **Report date:** 2021-02-03
- **Termination date:** 2021-02-11

- **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-1767-2020

## Citation

> AI Analytics. FDA recall Z-1767-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1767-2020. Source: US FDA. Licensed CC0.

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