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Physio-control Inc Recalls

28 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Physio-control Inc.

28Total Recalls
5Critical
457,192Units Affected
Apr 13, 2026Most Recent
All Recalls

Every Physio-control Inc Recall

Sorted by most recent. Click any recall for full details.

28 recalls
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-00...
Medical Devices·206 affected·Apr 13, 2026
High RiskFDA
Physio-control, Inc.
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalo...
Cardiac Devices·16,499 affected·Jan 21, 2026
High RiskFDA
Physio-control, Inc.
LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 defibrillator ...
Cardiac Devices·1 affected·Jul 22, 2025
High RiskFDA
Physio-control, Inc.
LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022...
Cardiac Devices·4 affected·Jul 22, 2025
High RiskFDA
Physio-control, Inc.
LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 88507469895...
Cardiac Devices·3 affected·Jul 22, 2025
High RiskFDA
Physio-control, Inc.
STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15 Defibrillation is indicat...
Cardiac Devices·3,617 affected·Aug 9, 2024
High RiskFDA
Physio-control, Inc.
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Cardiac Devices·18,732 affected·Nov 6, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Medical Devices·8 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001960, Part Number: V15-7-000026
Medical Devices·2 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602
Medical Devices·5 affected·Sep 29, 2023
RecallFDA
Physio-control, Inc.
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Cardiac Devices·1 affected·Jan 13, 2022
High RiskFDA
Physio-control, Inc.
LifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3011790-XXX/, U3011790-XXX - Product Usage: The L...
Cardiac Devices·173,459 affected·Mar 20, 2020
High RiskFDA
Physio-control, Inc.
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
Cardiac Devices·29,952 affected·Dec 20, 2019
High RiskFDA
Physio-control, Inc.
LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits
Cardiac Devices·705 affected·Dec 20, 2019
CriticalFDA
Physio-control Inc
LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care respo...
Cardiac Devices·13,005 affected·Feb 1, 2019
CriticalFDA
Physio-control Inc
LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardi...
Cardiac Devices·682 affected·Feb 1, 2019
CriticalFDA
Physio-control, Inc.
LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in the hospital, ...
Cardiac Devices·3,831 affected·Dec 4, 2017
CriticalFDA
Physio-control, Inc.
LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation electrodes are used only with LIFEPAK ...
Cardiac Devices·14,219 affected·Oct 27, 2017
High RiskFDA
Physio-control, Inc.
LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is used in various areas of the hospital such as critical area...
Cardiac Devices·7 affected·Jan 16, 2017
High RiskFDA
Physio-control, Inc.
LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medical personnel in out-of-doors and indo...
Cardiac Devices·2,584 affected·Jan 16, 2017
CriticalFDA
Physio-control, Inc.
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR...
Cardiac Devices·133,330 affected·Jan 13, 2017
High RiskFDA
Physio-control, Inc.
LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature installed. Part numbers: V15-2-xxxxxx (includes software versio...
Cardiac Devices·44,798 affected·Jan 27, 2016
High RiskFDA
Physio Control, Inc.
The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that uses a patented Shock Advisory System. This softw...
Cardiac Devices·139 affected·Jun 12, 2013
High RiskFDA
Physio-control, Inc.
The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor emergency care settings with...
Cardiac Devices·1,399 affected·Mar 11, 2010