Device recall
Z-0806-05: Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal…
FDA device recall · Class I · MRL, Inc., A Welch Allyn Company
Key facts
| Recall number (Z-number) | Z-0806-05 |
|---|---|
| Recall event | 31934 |
| Product | Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois 60089; Model AED20, part number 972200E |
| Product code | MKJ |
| Recalling firm | MRL, Inc., A Welch Allyn Company |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 1, 2006 |
| 510(k) numbers | K002232 |
| FEI number | 1418729 |
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