Device recall
Z-2834-2011: LuxStar Dental Light have the following Agency model or Catalog Model numbers as…
FDA device recall · Class II · Dental Equipment LLC
Key facts
| Recall number (Z-number) | Z-2834-2011 |
|---|---|
| Recall event | 59099 |
| Product | LuxStar Dental Light have the following Agency model or Catalog Model numbers as ML1000, OL1000, CL1000, WL1000, CB1000, TL1000, and UL1000. The product is labeled in part: " Marus Dental***Mfg By: Dental Equipment LLC.***705 S. Springbrook Rd Building C Newberg, Oregon, 97132 USA***Dental… |
| Product code | EAZ |
| Recalling firm | Dental Equipment LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 24, 2012 |
| FEI number | 1000523896 |
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