HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Reported: March 16, 2022 Initiated: January 13, 2022 #Z-0745-2022
Product Description
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.
Details
- Recalling Firm
- Physio-Control, Inc.
- Units Affected
- 1
- Distribution
- U.S.: AK
- Location
- Redmond, WA
Frequently Asked Questions
What product was recalled? ▼
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak. Recalled by Physio-Control, Inc.. Units affected: 1.
Why was this product recalled? ▼
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 16, 2022. Severity: Low. Recall number: Z-0745-2022.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11