--- title: "Physio-Control, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Physio-Control, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/physio-control-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Physio-Control, Inc. recall records **21** reported ongoing 22 records in this archive. Latest source date Apr 13, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Apr 13, 2026 FDA device enforcement ### [LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-...](https://isitonrecall.com/recall/fda-device-z-2065-2026-lifepak-15-ref-99577-000025-99577-000047-99577-001256-99577-001217-99577-001241-99577-001255-99577-0/) Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms s... Class II Reported ongoing Distribution: US Nationwide distribution in the states of MI, WA, KY, IN, FL, NC, TX, LA, VA, NY, MA, CO, PA, OH, SC, OK, MN, WV, NJ, WI. [Official source for LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-0012...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2065-2026%22) Jan 21, 2026 FDA device enforcement ### [PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 007219026...](https://isitonrecall.com/recall/fda-device-z-1544-2026-physio-control-infant-child-reduced-energy-defibrillator-electrodes-catalog-numbers-11101-000016-udi/) Due to pediatric defibrillator electrode delamination Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, N... [Official source for PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1544-2026%22) Jul 22, 2025 FDA device enforcement ### [LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020...](https://isitonrecall.com/recall/fda-device-z-2497-2025-lifepak-15-part-catalog-numbers-udi-di-code-v15-7-000022-99577-001957-883873871690-v15-2-000051-9957/) Due to required inspections not being performed on products/units that have gone through servicing. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CO and MT. [Official source for LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2497-2025%22) Jul 22, 2025 FDA device enforcement ### [LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 331706400001 / 99425-000025 / 8850746989...](https://isitonrecall.com/recall/fda-device-z-2498-2025-lifepak-1000-part-catalog-numbers-udi-di-code-320371500023-99425-000025-885074698953-320371500229-99/) Due to required inspections not being performed on products/units that have gone through servicing. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CO and MT. [Official source for LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2498-2025%22) Jul 22, 2025 FDA device enforcement ### [LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of ag...](https://isitonrecall.com/recall/fda-device-z-2499-2025-lifepak-cr2-part-catalog-numbers-udi-di-code-cr2-2-001451-99512-001434-883873785911-lifepak-cr2-the/) Due to required inspections not being performed on products/units that have gone through servicing. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CO and MT. [Official source for LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2499-2025%22) Feb 3, 2025 FDA device enforcement ### [LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.](https://isitonrecall.com/recall/fda-device-z-1232-2025-lifepak-20e-ref-99507-000001-the-aed-mode-is-to-be-used-only-on-patients-in-cardiopulmonary-arrest/) Incorrect keypad was incorrectly installed onto a defibrillator/monitor. Class II Reported ongoing Distribution: U.S.: WV O.U.S.: N/A [Official source for LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1232-2025%22) Jan 21, 2025 FDA device enforcement ### [LIFEPAK 35 ECG cable REF 11111-000041](https://isitonrecall.com/recall/fda-device-z-1102-2025-lifepak-35-ecg-cable-ref-11111-000041/) Product shipped with incorrect IFU. IFU does not include proper cleaning/disinfection instructions Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of CA, FL, GA, IA, IN, KY, MD, MI, MO, NE, NV, NY, OH, OR, SC, TN, TX, and WI. [Official source for LIFEPAK 35 ECG cable REF 11111-000041](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1102-2025%22) Jan 21, 2025 FDA device enforcement ### [LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF 11996-000515 Masimo¿ LNCS-II rainbow¿ DCI 8¿ SpCO, Adult Reusab...](https://isitonrecall.com/recall/fda-device-z-1184-2025-lifepak-15-v4-masimo-rainbow-sensors-masimo-rd-rainbow-adt-8-spco-spo2-and-spmet-adult-adhesive-sens/) Due to an error message that prevents users from utilizing carboxyhemoglobin saturation and methemoglobin saturation sensors on their monitor/defibrillator system. Class II Reported ongoing Distribution: U.S. Nationwide distribution including in the states of CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, MA, MD, MI, MO, MS, NC, NH, NY, OH, PA, SC, TN, TX, VA, WA, WI, and WV. [Official source for LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhe...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1184-2025%22) Aug 30, 2024 FDA device enforcement ### [LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000061 o 99577-000076 o 99577-001250 o 99577-001255 o 99577-001256 o 99577-001368 o...](https://isitonrecall.com/recall/fda-device-z-0230-2025-lifepak-15-lp15-model-catalog-numbers-o-97577-000101-o-99577-000046-o-99577-000055-o-99577-000061-o/) Due to an out of tolerance tool being used on monitor/defibrillator systems. Class II Reported ongoing Distribution: U.S.: CT, GA, MA, NY, OH, WA, and WV. O.U.S.: N/A [Official source for LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0230-2025%22) Aug 9, 2024 FDA device enforcement ### [STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15 Defibrillation is indicated for the termination of certain potentiall...](https://isitonrecall.com/recall/fda-device-z-0142-2025-sterilizable-internal-defibrillation-paddles-ref-lp20-sterilizable-internal-defibrillation-paddles-r/) Due to customer complaints and out of box failures, the firm is conducting a voluntary recall as a result of product failures (cracks and over-molding separation of the sterilizable internal defibrillation paddles. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, N... [Official source for STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0142-2025%22) Nov 6, 2023 FDA device enforcement ### [AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098](https://isitonrecall.com/recall/fda-device-z-0567-2024-ac-power-adapter-for-use-with-the-lifepak-15-monitor-defibrillator-ref-11140-000098/) AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM,... [Official source for AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0567-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051](https://isitonrecall.com/recall/fda-device-z-0296-2024-lifepak-15-ref-99577-000046-part-number-v15-2-000051/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0296-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-000055, Part Number V15-2-000061](https://isitonrecall.com/recall/fda-device-z-0297-2024-lifepak-15-ref-99577-000055-part-number-v15-2-000061/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-000055, Part Number V15-2-000061](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0297-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067](https://isitonrecall.com/recall/fda-device-z-0298-2024-lifepak-15-ref-99577-000061-part-number-v15-2-000067/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0298-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602](https://isitonrecall.com/recall/fda-device-z-0299-2024-lifepak-15-ref-99577-001255-part-number-v15-2-001602/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0299-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002](https://isitonrecall.com/recall/fda-device-z-0300-2024-lifepak-15-ref-99577-001373-part-number-v15-7-000002/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0300-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020](https://isitonrecall.com/recall/fda-device-z-0301-2024-lifepak-15-ref-99577-001955-part-number-v15-5-000584-and-v15-7-000020/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0301-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021](https://isitonrecall.com/recall/fda-device-z-0302-2024-lifepak-15-ref-99577-001956-part-number-v15-7-000021/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0302-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022](https://isitonrecall.com/recall/fda-device-z-0303-2024-lifepak-15-ref-99577-001957-part-number-v15-5-000586-and-v15-7-000022/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0303-2024%22) Sep 29, 2023 FDA device enforcement ### [LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023](https://isitonrecall.com/recall/fda-device-z-0304-2024-lifepak-15-ref-99577-001958-part-number-v15-7-000023/) Their is a potential for battery pins to become loose within the defibrillator resulting in power issues. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, NC, NJ, NY. [Official source for LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0304-2024%22) ## Reasons in these listed records - Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or ina... - Due to pediatric defibrillator electrode delamination - Due to required inspections not being performed on products/units that have gone through servicing. - Incorrect keypad was incorrectly installed onto a defibrillator/monitor. These examples come from this result page and are not a ranking of every recall reason. ## Checking Physio-Control, Inc. ### Is there a recall on physio-control, inc. right now? This archive contains 22 records, including 21 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Physio-Control, Inc.](https://isitonrecall.com/check/?q=Physio-Control%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)