Device recall
Z-0205-05: AccessAED PAD (without ECG trace) -Public Access Defibrillator Model Number…
FDA device recall · Class I · Access CardioSystems
Key facts
| Recall number (Z-number) | Z-0205-05 |
|---|---|
| Recall event | 30378 |
| Product | AccessAED PAD (without ECG trace) -Public Access Defibrillator Model Number: 9100-0010-0 |
| Product code | MKJ |
| Recalling firm | Access CardioSystems |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 12, 2006 |
| FEI number | 3003585458 |
At a glance
- None 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