Drug recall
ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for…
FDA recall event 94792 · Class II · Zoll Medical Corporation
Key facts
| Event ID | 94792 |
|---|---|
| Recall numbers | Z-2324-2024 |
| Recalling firm | Zoll Medical Corporation |
| Product type | Devices |
| Products | ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | G5 Semi-Automatic AED is shipped, with a protective film over its front panel, to protect the screen and shock button from cosmetic damage during shipping. It has come to our attention that customers… |
| Initiation date | May 31, 2024 |
| Report date | Jul 17, 2024 |
| City | Deerfield |
| State | WI |
| Country | United States |
| FEI number | 2112020 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: