Every recall we track for Physio-Control, Inc. — 33 in all — plus the complaints and injury reports the public filed about them.
Physio-Control recalls LIFEPAK 15 and other defibrillators serviced between July 2023 and November 2025 that may not function correctly due to missing performance inspections. Affected units require verification of service records.
Physio-Control recalls infant/child defibrillator electrodes with delamination risk. These electrodes may cause injury during emergency use. Affected units have specific catalog numbers and lot numbers.
Physio-Control recalls LIFEPAK 1000 defibrillators with specific catalog numbers due to required inspections not being performed after servicing. Affected units may pose risks if not properly maintained.
Physio-Control recalls LIFEPAK 15 defibrillators with specific catalog numbers due to required inspections not being performed after servicing. Affected units may have safety risks if not properly maintained.
Physio-Control recalls LIFEPAK CR2 defibrillators due to required inspections not being performed after servicing. Affected units have specific part numbers and serial codes. Consumers should contact the manufacturer for details.
Physio-Control recalls LIFEPAK 20e defibrillators with incorrect keypad installation that may not function properly during cardiac emergencies.
Physio-Control recalls LIFEPAK 35 ECG cable REF 11111-000041 due to missing cleaning instructions in user manual. Affected units shipped with incorrect instructions.
Physio-Control recalls LIFEPAK 15 V4 and Masimo Rainbow Sensors due to an error message blocking carboxyhemoglobin and methemoglobin saturation readings. Affected units include specific model numbers and lot numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with specific model numbers due to an out of tolerance tool used during manufacturing, potentially causing system failure.
Physio-Control recalls sterilizable defibrillation paddles LP20 and LP15 due to cracks and over-molding separation causing product failures. Affected units may have safety risks during medical use.
Physio-Control recalls AC power adapters for LIFEPAK 15 defibrillators that may not charge batteries or power on when plugged in. Affected units were made between November 2021 and April 2023.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power problems. Affected units have specific serial numbers and part numbers. Consumers should contact the company for details.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin loosening causing power problems. Affected units have specific serial numbers and part numbers. Contact for repair or replacement.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin loosening causing power problems. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin issues causing power problems. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-Control recalls HeartSine Samar: Defibrillators shipped without battery packs. Users must check serial numbers to confirm if affected. No remedy details provided in recall notice.
Physio-Control
Physio-Control recalls infant/child reduced energy defibrillation electrodes (part number 3202380-006) for use with LIFEPAK 1000, 500, and CR Plus/EXPRESS defibrillators due to improperly sealed packaging. This could lead to contamination or damage.
Physio-Control recalls Infant Child Starter Kits (part 3202784-009) with improperly sealed packaging for infant/child defibrillation electrodes, which could lead to contamination. Affected kits were sold from August 2017 to October 2019.
Physio-Control recalls LifePAK 500 AEDs with specific model numbers due to risk of failing to detect patient connection, potentially delaying critical cardiac treatment.
Physio-Control recalls LIFEPAK 15 Monitor/Defibrillators with serial numbers listed that may lock up after a shock delivery, causing blank display with LED lights on but no response. Affected units should be checked for serial numbers in the list.
Physio-Control
Physio-Control
Physio-Control recalls LIFEPAK defibrillation electrodes (Catalog # 11101-000016) due to incorrect pad placement instructions and missing safety symbols. Affected units sold in specific model numbers.
Physio-Control recalls LIFEPAK Electrode Starter Kits with incorrect infant pad placement instructions and missing safety symbols. Consumers should check product details to avoid improper use during emergencies.
