Device recall
Z-0691-2013: Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment…
FDA device recall · Class II · Quanta System, S.p.A.
Key facts
| Recall number (Z-number) | Z-0691-2013 |
|---|---|
| Recall event | 64039 |
| Product | Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented lesions; Hair and tattoo removal; The incision, excision, ablation, vaporization of soft tissue for general dermatology. Ruby 694nm: Cutting, vaporization and ablation of soft tissue… |
| Product code | GEX |
| Recalling firm | Quanta System, S.p.A. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 23, 2013 |
| 510(k) numbers | K073549, K123168 |
| FEI number | 3004378299 |
At a glance
- 1–9 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