---
title: "HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad... — FDA record Z-0745-2022 | Is It on Recall"
description: "Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs."
url: https://isitonrecall.com/recall/fda-device-z-0745-2022-heartsine-samaritan-pad-sam-350p-semi-automatic-defibrillator-used-with-pad-pak/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak — FDA record Z-0745-2022

Reported terminated

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 Jan 13, 2022. 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**: HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
- **Reason**: Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
- **Classification**: Class III
- **Recalling firm**: Physio-Control, Inc.
- **Quantity**: 1
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0745-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0745-2022%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 | GTIN/UDI: 05060167120695, Serial Number: 20D00009694 |

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

## Distribution

U.S.: AK

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

- [Alaska](https://isitonrecall.com/state/alaska/)

## Dates in the source

- **Report date**: Mar 16, 2022
- **Recall initiation date**: Jan 13, 2022
- **Center classification date**: Mar 10, 2022
- **Termination date**: May 19, 2023

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-0745-2022%22)

## Related records

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