Device recall
Z-0321-06: HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation…
FDA device recall · Class III · Philips Medical Systems
Key facts
| Recall number (Z-number) | Z-0321-06 |
|---|---|
| Recall event | 34045 |
| Product | HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads Model M3717A |
| Product code | MLN |
| Recalling firm | Philips Medical Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 12, 2006 |
| 510(k) numbers | K003228 |
| FEI number | 1218950 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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