---
title: "MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysi... — FDA record Z-2306-2026 | Is It on Recall"
description: "Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the"
url: https://isitonrecall.com/recall/fda-device-z-2306-2026-mac-5-a4-resting-ecg-analysis-system-855001-001-mac-5-a5-resting-ecg-analysis-system-8855002-001-ele/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph — FDA record Z-2306-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 21, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
- **Reason**: Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.
- **Classification**: Class II
- **Recalling firm**: GE Medical Systems China Co., Ltd.
- **Quantity**: 16
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2306-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2306-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Software version 3.00 855001-001, UDI-DI 00195278276070 8855002-001, UDI-DI 00195278276124 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the states of Florida and Georgia. The countries of India, Italy, Republic of Korea, and United Kingdom.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jun 10, 2026
- **Recall initiation date**: Apr 21, 2026
- **Center classification date**: Jun 3, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2306-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [GE Medical Systems China Co., Ltd. records](https://isitonrecall.com/brand/ge-medical-systems-china-co-ltd/)
