Device recall
Z-0357-04: Coherent brand Quattro Diode Laser Systems; A Quattro FAP System; Model…
FDA device recall · Class II · Coherent Inc Laser Group
Key facts
| Recall number (Z-number) | Z-0357-04 |
|---|---|
| Recall event | 28434 |
| Product | Coherent brand Quattro Diode Laser Systems; A Quattro FAP System; Model Numbers/Serial Numbers: TFAP0004P--TFAP00048 |
| Product code | -- |
| Recalling firm | Coherent Inc Laser Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 8, 2005 |
| FEI number | 2916213 |
At a glance
- None 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