---
title: "LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in c... — FDA record Z-1232-2025 | Is It on Recall"
description: "Incorrect keypad was incorrectly installed onto a defibrillator/monitor."
url: https://isitonrecall.com/recall/fda-device-z-1232-2025-lifepak-20e-ref-99507-000001-the-aed-mode-is-to-be-used-only-on-patients-in-cardiopulmonary-arrest/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest. — FDA record Z-1232-2025

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 Feb 3, 2025. 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**: LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
- **Reason**: Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
- **Classification**: Class II
- **Recalling firm**: Physio-Control, Inc.
- **Quantity**: 1
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1232-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1232-2025%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 | Model/Catalog Number: 99507-000001 UDI-DI code: 00883873813751 Serial Number: 38289467 |

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

## Distribution

U.S.: WV O.U.S.: N/A

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

- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Mar 5, 2025
- **Recall initiation date**: Feb 3, 2025
- **Center classification date**: Feb 25, 2025

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-1232-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Physio-Control, Inc. records](https://isitonrecall.com/brand/physio-control-inc/)