Z-0745-2022 Class III Terminated
FDA device recall Z-0745-2022 was initiated by Physio-Control, Inc. on Jan 13, 2022 and is designated Class III. Reason for recall: Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs. The recall status is terminated (terminated May 19, 2023). Affected quantity: 1.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 16, 2022
- Initiation Date
- Jan 13, 2022
- Termination Date
- May 19, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
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.
Distribution Pattern
U.S.: AK
Code Information
GTIN/UDI: 05060167120695, Serial Number: 20D00009694
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0745-2022
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026