Device recall
Z-0587-2010: SoftLase Pro Dental Lasers: Zap SoftLase, SoftLase Pro, OrthoLase, and…
FDA device recall · Class II · Zap Lasers LLC
Key facts
| Recall number (Z-number) | Z-0587-2010 |
|---|---|
| Recall event | 54153 |
| Product | SoftLase Pro Dental Lasers: Zap SoftLase, SoftLase Pro, OrthoLase, and HygieneLase models, Model numbers ZA-SLP, ZA-ORT, ZA-HYG, G22002SLP, ZA-SOFTLASE2WSII, ZA-SOFTLASER2W, Manufactured by Zap Lasers LLC, Pleasant Hill, CA. Intended use: Dentistry. |
| Product code | NVK |
| Recalling firm | Zap Lasers LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 25, 2010 |
| FEI number | 3005212363 |
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