Drug recall
Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual…
FDA recall event 96653 · Class II · Defibtech, LLC
Key facts
| Event ID | 96653 |
|---|---|
| Recall numbers | Z-1694-2025 |
| Recalling firm | Defibtech, LLC |
| Product type | Devices |
| Products | Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual language) |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use)… |
| Initiation date | Mar 18, 2025 |
| Report date | May 7, 2025 |
| City | Guilford |
| State | CT |
| Country | United States |
| FEI number | 3003521780 |
At a glance
- 1–9 Products in this recall
- 1–9 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: