Device recall
Z-0918-04: Welch Allyn AED 10 Defibrillator; a battery powered automated external…
FDA device recall · Class II · MRL, Inc., A Welch Allyn Company
Key facts
| Recall number (Z-number) | Z-0918-04 |
|---|---|
| Recall event | 28880 |
| Product | Welch Allyn AED 10 Defibrillator; a battery powered automated external defibrillator; Manufacturer: MRL, Inc., A Welch Allyn Company, 100 Asbury Drive, Buffalo Grove, Illinois 60089; Model AED10, part numbers 970300 (defibrillator) and 970302 (defibrillator with soft shell carrying case) |
| Product code | MKJ-- |
| Recalling firm | MRL, Inc., A Welch Allyn Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2004 |
| 510(k) numbers | K021168 |
| FEI number | 1418729 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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