FDAFDA · Food and drugs·Recall number Z-0745-2022
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Published March 16, 2022 · Recall initiated: January 13, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Physio-Control, Inc.
- Distributor
- U.S.: AK
- Lot
- GTIN/UDI: 05060167120695, Serial Number: 20D00009694
- Risk classification
- Class III
- Area (FDA)
- device
- Country
- United States
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