Device recall
Z-1170-2010: LM Aculight Corporation Perseus Pulsed Fiber Laser, Model number: ML36L-1541…
FDA device recall · Class II · Lockheed-Martin Aculight
Key facts
| Recall number (Z-number) | Z-1170-2010 |
|---|---|
| Recall event | 54087 |
| Product | LM Aculight Corporation Perseus Pulsed Fiber Laser, Model number: ML36L-1541. Additional Model numbers with non-defective type"A" fiber: M22L-1540, M27L-1541, M281-1540, M30PL-1541, & M33L-1541. Lockheed Martin Aculight, Bothell, WA, 98021. Pulsed laser energy generator intended for use as an OEM… |
| Product code | RDW |
| Recalling firm | Lockheed-Martin Aculight |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 30, 2012 |
| 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