Device recall
Z-2069-2011: Lockheed Martin Aculight Capella-r 1850 Laser. This device has the Accession…
FDA device recall · Class II · Lockheed-Martin Aculight
Key facts
| Recall number (Z-number) | Z-2069-2011 |
|---|---|
| Recall event | 57473 |
| Product | Lockheed Martin Aculight Capella-r 1850 Laser. This device has the Accession number 0612339. The Capella R-1850 is a Class 4 solid state diode laser product designed to emit 1850mn laser radiation at maximum pulse energy of 5 mJ (@1ms). The output port connects to a user-selected 200-600 micron… |
| Product code | RGB |
| Recalling firm | Lockheed-Martin Aculight |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2011 |
| FEI number | 3003346474 |
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