HeartSine Samaritan PAD — Class III medical device recall Z-0745-2022
Terminated recall by Physio-Control, Inc., reported 2022-03-16, distributed in AK. Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
| Recall number | Z-0745-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2022-01-13 |
| Classified | 2022-03-10 |
| Reported by FDA | 2022-03-16 |
| Terminated | 2023-05-19 |
| Distributed | AK |
| Quantity | 1 |
| UPC / GTIN / UDI-DI | 05060167120695 |
| Serial numbers | 20D00009694 |
Product
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Reason for recall
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0745-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.