Physio-Control, Inc. recalls
Every recall we track for Physio-Control, Inc. — 33 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Physio-Control, Inc. more than tripled in 2025 (6, up from 2 in 2024). 3% rated “stop using now”.
All FDA recall records for Physio-Control, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 2 | 1 | 0 | 3 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 2 | 2 | 0 | 4 |
| 2020 | 0 | 1 | 2 | 0 | 3 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 0 | 0 | 1 |
| 2023 | 0 | 2 | 9 | 0 | 11 |
| 2024 | 0 | 2 | 0 | 0 | 2 |
| 2025 | 0 | 1 | 4 | 1 | 6 |
| 2026 (to date) | 0 | 2 | 0 | 0 | 2 |
Most common reasons for Physio-Control, Inc. recalls
What to do if you have a recalled Physio-Control, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Physio-Control, Inc. recalls
18 shown- Use cautionMedical device
Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,
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-ControlApr 13, 2026 - Use cautionMedical device
Physio-Control, Inc. recalls PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:
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-ControlJan 21, 2026 - UnratedMedical device
Physio-Control, Inc. recalls LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2
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-ControlJul 22, 2025 - Use cautionMedical device
Physio-Control, Inc. recalls LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Physio-Control recalls LIFEPAK 20e defibrillators with incorrect keypad installation that may not function properly during cardiac emergencies.
Physio-ControlFeb 3, 2025 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 35 ECG cable REF 11111-000041
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-ControlJan 21, 2025 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF
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-ControlJan 21, 2025 - Use cautionMedical device
Physio-Control, Inc. recalls LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000061 o 99577-000076 o
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-ControlAug 30, 2024 - Use cautionMedical device
Physio-Control, Inc. recalls STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15
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-ControlAug 9, 2024 - Lower riskMedical device
Physio-Control, Inc. recalls AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
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-ControlNov 6, 2023 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051
Physio-Control recalls LIFEPAK 15 defibrillators with potential battery pin looseness causing power issues. Affected units have specific serial numbers and part numbers.
Physio-ControlSep 29, 2023 - Stop using nowMedical device
Physio-Control, Inc. recalls HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
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-ControlJan 13, 2022 - Lower riskMedical device
Physio-Control, Inc. recalls PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor
Physio-Control
Physio-ControlJan 14, 2021 - Lower riskMedical device
Physio-Control, Inc. recalls Infant Child Starter Kits, Part Number: 3202784-009, containing Infant/Child Reduced Energy Defibrillation Electrodes,
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-ControlApr 24, 2020 - Use cautionMedical device
Physio-Control, Inc. recalls LifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3011790-XXX/, U3011790-XXX -
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-ControlMar 20, 2020 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an
Physio-Control
Physio-ControlDec 20, 2019 - Lower riskMedical device
Physio-Control Inc recalls LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute
Physio-Control
Physio-ControlFeb 1, 2019 - Lower riskMedical device
Physio-Control, Inc. recalls LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in
Physio-Control
Physio-ControlDec 4, 2017 - Use cautionMedical device
Physio-Control, Inc. recalls LIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation electrodes are used only
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.
Physio-ControlOct 27, 2017
Physio-Control, Inc. recall questions
How many recalls has Physio-Control, Inc. had?
33 recalls from Physio-Control, Inc. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Physio-Control, Inc. recall?
Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,, dated Apr 13, 2026. Every Physio-Control, Inc. recall is listed on this page, newest first.
Why are Physio-Control, Inc. products recalled?
The most common reasons on record: Packaging of infant child reduced energy electrodes was not properly sealed. (2).
What should I do if I have a recalled Physio-Control, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Physio-Control, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.