Device recall
Z-1005-2009: Welch Allyn AED 10 Automated External Defibrillator
FDA device recall · Class I · Welch Allyn Protocol, Inc
Key facts
| Recall number (Z-number) | Z-1005-2009 |
|---|---|
| Recall event | 50142 |
| Product | Welch Allyn AED 10 Automated External Defibrillator |
| Product code | MKJ |
| Recalling firm | Welch Allyn Protocol, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 15, 2012 |
| 510(k) numbers | K021168 |
| FEI number | 3023750 |
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