Device recall
Z-2035-2008: Physio-Control Internal Defibrillator Handles. PN: 3010901-002 for use with…
FDA device recall · Class II · Physio Control, Inc.
Key facts
| Recall number (Z-number) | Z-2035-2008 |
|---|---|
| Recall event | 46749 |
| Product | Physio-Control Internal Defibrillator Handles. PN: 3010901-002 for use with LIFEPAK 12 and 20. PN: 805249-014 thru 019 for use with LIFEPAK 9 and 9P. |
| Product code | LDD |
| Recalling firm | Physio Control, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2011 |
| 510(k) numbers | K895379 |
| 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