Device recall
Z-1188-2012: Aerolase Corporation. The products involved are the FriendlyLight YAG lasers, a…
FDA device recall · Class II · Aerolase
Key facts
| Recall number (Z-number) | Z-1188-2012 |
|---|---|
| Recall event | 61194 |
| Product | Aerolase Corporation. The products involved are the FriendlyLight YAG lasers, a Model Family first identified and reported. The products are marketed under names including FriendlyLight Er:YAG, LightPod Era, FriendlyLight Nd:YAG, LightPod Neo, LightPod Neo XL, LightPod Neo XT, LightPod Forte… |
| Product code | GEX |
| Recalling firm | Aerolase |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2018 |
| FEI number | 3004374705 |
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