Device recall
Z-0077-2011: DDC-6-AA Data Card, an accessory to the Sentry DDU-1 00 semiautomatic external…
FDA device recall · Class II · Defibtech, LLC
Key facts
| Recall number (Z-number) | Z-0077-2011 |
|---|---|
| Recall event | 56729 |
| Product | DDC-6-AA Data Card, an accessory to the Sentry DDU-1 00 semiautomatic external defibrillator (AED). The DDC-6-AA data card is an accessory to the AED and does not have its own intended use. |
| Product code | MKJ |
| Recalling firm | Defibtech, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2011 |
| 510(k) numbers | K013896 |
| FEI number | 3003521780 |
At a glance
- 1–9 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