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Physio-Control, Inc. recalls HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Recalled March 16, 2022 · FDA recall Z-0745-2022 · Physio-Control
Hazard
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs. · FDA Class III
Units
1
Sold at
U.S.: AK
Description
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
Product
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Manufacturer(s)
Physio-Control, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →