Physio-Control, Inc. recalls

10 recalls on record · latest: April 13, 2026

Official U.S. recall history for Physio-Control, Inc., compiled from official government records.

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Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 9957…

April 13, 2026 · Medical device recalls Moderate risk Some defibrillators serviced between July 2023 through November 2025 were servi…

Physio-Control, Inc. recalls PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902…

January 21, 2026 · Medical device recalls Moderate risk Due to pediatric defibrillator electrode delamination

Physio-Control, Inc. recalls LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-0000…

July 22, 2025 · Medical device recalls Moderate risk Due to required inspections not being performed on products/units that have gon…

Physio-Control, Inc. recalls LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046…

July 22, 2025 · Medical device recalls Moderate risk Due to required inspections not being performed on products/units that have gon…

Physio-Control, Inc. recalls LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 d…

July 22, 2025 · Medical device recalls Moderate risk Due to required inspections not being performed on products/units that have gon…

Physio-Control, Inc. recalls LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.

February 3, 2025 · Medical device recalls Moderate risk Incorrect keypad was incorrectly installed onto a defibrillator/monitor.

Physio-Control, Inc. recalls LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF 11996…

January 21, 2025 · Medical device recalls Moderate risk Due to an error message that prevents users from utilizing carboxyhemoglobin sa…

Physio-Control, Inc. recalls LIFEPAK 35 ECG cable REF 11111-000041

January 21, 2025 · Medical device recalls Moderate risk Product shipped with incorrect IFU. IFU does not include proper cleaning/disinf…

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 9…

August 30, 2024 · Medical device recalls Moderate risk Due to an out of tolerance tool being used on monitor/defibrillator systems.

Physio-Control product recalled over mold contamination

August 9, 2024 · Medical device recalls Moderate risk Due to customer complaints and out of box failures, the firm is conducting a vo…