Device recall
Z-2180-2008: Impax 6.x Clients including: 6.3 all versions below 6.3.1 SU5, 6.2 all versions…
FDA device recall · Class III · AGFA Corp.
Key facts
| Recall number (Z-number) | Z-2180-2008 |
|---|---|
| Recall event | 48632 |
| Product | Impax 6.x Clients including: 6.3 all versions below 6.3.1 SU5, 6.2 all versions below 6.2.1 SU14 and 6.0 all versions. The Impax Systems are Picture Archiving and Communications system (PACs). PAC systems are used in the acceptance, transfer, display, storage and digital processing of medical… |
| Product code | LLZ |
| Recalling firm | AGFA Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 9, 2009 |
| 510(k) numbers | K022292 |
| FEI number | 3001236302 |
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