Device recall
Z-1692-2025: Automated External Defibrillators, Model DDU-2300. Item numbers…
FDA device recall · Class II · Defibtech, LLC
Key facts
| Recall number (Z-number) | Z-1692-2025 |
|---|---|
| Recall event | 96618 |
| Product | Automated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1(German/English dual language), DCF-E2310E3/1(German/French dual language), DCF-E2310F3/1 (French/English dual language), DCF-E2310G3/1(French/German dual language), DCF-E2310IT (Italian language) |
| Product code | MKJ |
| Recalling firm | Defibtech, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P160032 |
| FEI number | 3003521780 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database