Device recall
Z-2311-2010: External Sterilizable Paddles for use with the LIFEPAK 9, LIFEPAK 9P, LIFEPAK…
FDA device recall · Class II · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-2311-2010 |
|---|---|
| Recall event | 50214 |
| Product | External Sterilizable Paddles for use with the LIFEPAK 9, LIFEPAK 9P, LIFEPAK 12, and LIFEPAK 20/20e Defibrillator/Monitor. |
| Product code | LDD |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 28, 2010 |
| 510(k) numbers | K902288 |
| FEI number | 3015876 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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