Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: — Class II medical device recall Z-1320-2025
Ongoing recall by ZOLL Medical Corporation, reported 2025-03-19, distributed nationwide. The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (t
| Recall number | Z-1320-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ZOLL Medical Corporation, Chelmsford, MA, United States |
| Recall initiated | 2025-02-13 |
| Classified | 2025-03-12 |
| Reported by FDA | 2025-03-19 |
| Distributed | Nationwide (US) |
| Quantity | 73 units |
| UPC / GTIN / UDI-DI | 00812394021246 |
| Serial numbers | D00000004687, D00000004688, D00000005214, D00000017929, D00000067528, D00000067585, D00000067595, D00000067685, D00000089561, D00000089566, D00000089577, D00000105587, D00000111542, D00000111556, D00000111640, D00000111706, D00000111718, D00000113136, D00000113147, D00000113175, D00000113177, D00000113178, D00000113180, D00000113181, D00000113182 and 47 more |
| Model numbers | 00812394021246, G5S-01C, G5S-02C, G5S-10C, G5S-11C |
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; 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 for recall
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1320-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.