Class II FDA device recall · Z-1322-2025

Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.

This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.

Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9) G5S-80-L (10) G5S-90A; 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.

Why it was recalled

The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).

Is your unit affected?

The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.

A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.

Show the FDA's listed lot / code information

Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9)G5S-80-L, (10) G5S-90A; UDI-DI: (1) no UDI, (2) 00812394021239, (3) no UDI, (4) no UDI, (5) no UDI, (6) no UDI, (7) no UDI, (8) 00812394021413, (9) no UDI, (10) no UDI; Serial Numbers: (1) D00000154575, D00000154617,      (2) D00000003725, D00000003727, D00000003734, D00000003896, D00000003898, D00000003923, D00000003927, D00000003941, D00000003943, D00000003951, D00000003955, D00000003962, D00000003964, D00000003965, D00000003968, D00000003971, D00000003972, D00000003981, D00000003982, D00000003984, D00000003987, D00000003989, D00000003991, D00000003997, D00000003999, D00000004149, D00000004151, D00000004153, D00000004154, D00000004156, D00000004158, D00000004301, D00000004304, D00000004308, D00000004313, D00000004324, D00000004329, D00000004365, D00000004390, D00000004394, D00000004402, D00000004407, D00000004408, D00000004410, D00000004413, 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D00000191367, D00000191368, D00000191369, D00000191371, D00000191372, D00000191380, D00000191382, D00000191383, D00000191386, D00000191387, D00000191388, D00000191390, D00000191391, D00000191393, D00000191395, D00000191397, D00000191399, D00000191400, D00000191401, D00000191402, D00000191406, D00000191408, D00000191409, D00000191410, D00000191412, D00000191413, D00000191414, D00000191417, D00000191419, D00000191420, D00000191422, D00000191423, D00000191424, D00000191425, D00000191426, D00000191427, D00000191441, D00000191442, D00000191443, D00000191458, D00000191739, D00000191769, D00000191770, D00000191784, D00000192920, D00000193403, D00000193419, D00000193426, D00000193431, D00000193437, D00000194387, D00000194404, D00000195671, D00000203930, D00000223520, D00000223583, D00000223589, D00000223592, D00000223595, D00000223596, D00000223607, D00000223608, D00000223614, D00000223626, D00000224270, D00000224285, D00000240832, D00000252303, D00000270197, D00000270242, D00000270244, D00000270265, M00000002042, M00000015317, M00000015355, M00000015411, M00000015413, M00000015416, M00000015420, M00000015480, M00000015489, M00000015540, M00000015544, M00000015557, M00000015576, M00000015642, M00000015677, M00000015696, M00000015748, M00000015781, M00000015812, M00000015818, M00000015819, M00000015890, M00000015895, M00000015902, M00000015919, M00000015923, M00000015960, M00000015965,      (3) D00000002496, D00000195191,     (4) D00000228356,      (5) D00000095452,     (6) D00000023456, M00000001511,      (7) M00000006322,     (8) D00000247707, D00000247709, D00000247717, D00000247721, D00000247722, D00000247723, D00000247724, D00000247725, D00000247726, D00000247728, D00000247738, D00000247741, D00000247786, D00000247792, D00000247796, D00000247803, D00000247805, D00000247806,      (9) D00000025111, D00000029078,       (10) D00000035676, D00000176940;

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

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.

Recall record

Recalling firm: ZOLL Medical Corporation
Product type: Devices
Recall number: Z-1322-2025
Voluntary / mandated: Voluntary: Firm initiated
Initial notification: Letter
Origin: Chelmsford, MA
Recall initiated: 2025-02-13

What to do

Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.

Also available: structured data (JSON-LD) · recall record (JSON)

What this is — and is not

A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.

To report a problem you experienced, use FDA MedWatch. Verify this record at FDA recalls · Recall Z-1322-2025 · Source: openFDA enforcement.