Device recall
Z-1223-2007: Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal…
FDA device recall · Class I · Welch Allyn Protocol, Inc
Key facts
| Recall number (Z-number) | Z-1223-2007 |
|---|---|
| Recall event | 39368 |
| Product | Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, Buffalo Grove, Illinois; Model AED 20, Catalog Numbers 972213, 972214, 972215, 972216 (Part Numbers 972200E, 972211E, 972212E, 972213E… |
| Product code | MKJ |
| Recalling firm | Welch Allyn Protocol, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 26, 2011 |
| 510(k) numbers | K002232 |
| 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