--- title: "Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5... — FDA record Z-1318-2025 | Is It on Recall" description: "The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity)." url: https://isitonrecall.com/recall/fda-device-z-1318-2025-brand-name-zoll-product-name-powerheart-g5-aed-model-catalog-number-1-g5a-80c-2-g5a-80c-tso-software/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80C, (2) G5A-80C-TSO. Software Version... — FDA record Z-1318-2025 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Feb 13, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. 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/). ## What the record says - **Product**: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80C, (2) G5A-80C-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA). There are two models available fully automatic and semi-automatic. After the defibrillations pads are applied to the patient, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is detected, delivers a shock without any rescuer assistance. The semi-automatic model evaluates the heart rhythm and requires the rescuer to press the shock button if a shockable rhythm is detected. Both models have voice and text instructions that guide the rescuer through the entire defibrillation process. Note: Not all configurations described in this document are available in all areas. - **Reason**: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity). - **Classification**: Class II - **Recalling firm**: ZOLL Medical Corporation - **Quantity**: 63,607 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-1318-2025 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1318-2025%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | Model/Catalog Number: (1) G5A-80C, (2) G5A-80C-TSO; UDI-DI: (1) 00812394021208, (2) 00812394021406; Serial Numbers: (1) D00000022708, D00000033165, D00000033168, D00000033171, D00000033174, D00000033185, D00000033187, D00000033189, D00000033191, D00000033208, D00000033209, D00000033211, D00000033213, D00000033214, D00000033216, D00000033217, D00000033219, D00000033220, D00000033221, D00000033222, D00000033230, D00000035201, D00000035208, D00000035246, D00000035445, D00000035512, D00000035517, D00000035521, D00000035523, D00000035524, D00000035525, D00000035528, D00000035530, D00000035532, D00000035534, D00000035536, D00000035538, D00000035539, D00000035542, D00000035544, D00000035546, D00000035548, D00000035549, D00000035554, D00000035558, D00000035560, D00000035562, D00000035584, 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D00000046527, D00000046532, D00000046533, D00000046550, D00000046553, D00000046559, D00000046562, D00000046564, D00000046565, D00000046568, D00000046569, D00000046580, D00000046585, D00000046586, D00000046587, D00000046589, D00000046592, D00000046597, D00000046599, D00000046600, D00000046626, D00000046627, D00000046630, D00000046661, D00000046663, D00000046667, D00000046669, D00000046689, D00000046692, D00000046694, D00000046695, D00000046697, D00000046699, D00000046701, D00000046703, D00000046705, D00000046707, D00000046710, D00000047180, D00000047189, D00000047198, D00000047201, D00000047212, D00000047230, D00000047231, D00000047232, D00000047233, D00000047234, D00000047235, D00000047239, D00000047246, D00000047253, D00000047260, D00000047277, D00000047287, D00000047289, D00000047297, D00000047308, D00000047310, D00000047336, D00000047337, D00000047338, D00000047339, D00000047340, D00000047344, D00000047345, D00000047348, D00000047350, D00000047426, D00000047427, D00000047483, D00000047557, D00000047563, D00000047564, D00000047567, D00000047571, D00000047590, D00000047591, D00000047596, D00000047601, D00000047603, D00000047607, D00000047610, D00000047642, D00000047670, D00000047691, D00000047696, D00000047716, D00000047718, D00000047723, D0000... | The agency lot list is longer than this excerpt. [Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1318-2025%22). Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution Domestic: Nationwide Distribution International: AE, AI, AM, AR, AT, AU, BD, BE, BG, BH, BM, BN, BS, CA, CH, CL, CN, CO, CR, CZ, DE, DK, DO, EG, ES, FI, FR, GB, GH, GU, HK, HR, HU, ID, IE, IL, IN, IS, IT, JE, JM, JP, KR, KW, KZ, LB, LT, MA, MC, MD, ME, MQ, MS, MT, MX, MY, NC, NG, NL, NO, NZ, OM, PA, PE, PG, PH, PK, PL, PR, PT, QA, RE, RO, RS, RU, SA, SE, SG, SI, SK, SM, TC, TH, TN, TR, TW, UA, US, VG, ZA. States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address. - [Alaska](https://isitonrecall.com/state/alaska/) - [Alabama](https://isitonrecall.com/state/alabama/) - [Arkansas](https://isitonrecall.com/state/arkansas/) - [Arizona](https://isitonrecall.com/state/arizona/) - [California](https://isitonrecall.com/state/california/) - [Colorado](https://isitonrecall.com/state/colorado/) - [Connecticut](https://isitonrecall.com/state/connecticut/) - [Delaware](https://isitonrecall.com/state/delaware/) - [Florida](https://isitonrecall.com/state/florida/) - [Georgia](https://isitonrecall.com/state/georgia/) - [Hawaii](https://isitonrecall.com/state/hawaii/) - [Iowa](https://isitonrecall.com/state/iowa/) - [Idaho](https://isitonrecall.com/state/idaho/) - [Illinois](https://isitonrecall.com/state/illinois/) - [Indiana](https://isitonrecall.com/state/indiana/) - [Kansas](https://isitonrecall.com/state/kansas/) - [Kentucky](https://isitonrecall.com/state/kentucky/) - [Louisiana](https://isitonrecall.com/state/louisiana/) - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Maryland](https://isitonrecall.com/state/maryland/) - [Maine](https://isitonrecall.com/state/maine/) - [Michigan](https://isitonrecall.com/state/michigan/) - [Minnesota](https://isitonrecall.com/state/minnesota/) - [Missouri](https://isitonrecall.com/state/missouri/) - [Mississippi](https://isitonrecall.com/state/mississippi/) - [Montana](https://isitonrecall.com/state/montana/) - [North Carolina](https://isitonrecall.com/state/north-carolina/) - [North Dakota](https://isitonrecall.com/state/north-dakota/) - [Nebraska](https://isitonrecall.com/state/nebraska/) - [New Hampshire](https://isitonrecall.com/state/new-hampshire/) - [New Jersey](https://isitonrecall.com/state/new-jersey/) - [New Mexico](https://isitonrecall.com/state/new-mexico/) - [Nevada](https://isitonrecall.com/state/nevada/) - [New York](https://isitonrecall.com/state/new-york/) - [Ohio](https://isitonrecall.com/state/ohio/) - [Oklahoma](https://isitonrecall.com/state/oklahoma/) - [Oregon](https://isitonrecall.com/state/oregon/) - [Pennsylvania](https://isitonrecall.com/state/pennsylvania/) - [Rhode Island](https://isitonrecall.com/state/rhode-island/) - [South Carolina](https://isitonrecall.com/state/south-carolina/) - [South Dakota](https://isitonrecall.com/state/south-dakota/) - [Tennessee](https://isitonrecall.com/state/tennessee/) - [Texas](https://isitonrecall.com/state/texas/) - [Utah](https://isitonrecall.com/state/utah/) - [Virginia](https://isitonrecall.com/state/virginia/) - [Vermont](https://isitonrecall.com/state/vermont/) - [Washington](https://isitonrecall.com/state/washington/) - [Wisconsin](https://isitonrecall.com/state/wisconsin/) - [West Virginia](https://isitonrecall.com/state/west-virginia/) - [Wyoming](https://isitonrecall.com/state/wyoming/) ## Dates in the source - **Report date**: Mar 19, 2025 - **Recall initiation date**: Feb 13, 2025 - **Center classification date**: Mar 12, 2025 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1318-2025%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [ZOLL Medical Corporation records](https://isitonrecall.com/brand/zoll-medical-corporation/)