Device recall
Z-0503-2025: Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models…
FDA device recall · Class II · Defibtech, LLC
Key facts
| Recall number (Z-number) | Z-0503-2025 |
|---|---|
| Recall event | 95594 |
| Product | Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.) |
| 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