FDA Device recall Z-0745-2022
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
- FDA Device
- Class III
- terminated
- Published 2022-03-16
On 2022-03-16 the FDA classified a Class III recall of HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak by Physio Control, citing semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0745-2022 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2022-01-13 |
| Published | 2022-03-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Physio Control |
| Distribution | AK |
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.
Identifiers
| code_info | GTIN/UDI: 05060167120695, Serial Number: 20D00009694 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0745-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.