Device recall
Z-1998-2009: Ultra-Thin LightMat Surgical Illuminator, Disposable one time use. Model Number…
FDA device recall · Class II · Lumitex Inc
Key facts
| Recall number (Z-number) | Z-1998-2009 |
|---|---|
| Recall event | 52817 |
| Product | Ultra-Thin LightMat Surgical Illuminator, Disposable one time use. Model Number: UA2550, Exp Date: 2012-05. Product is packaged in individual sterile pouch w/5 pouches per box. The LightMat is intended for the illumination of surgical procedures, particularly where deep cavities or adjacent tissues… |
| Product code | FDG |
| Recalling firm | Lumitex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2012 |
| FEI number | 1000122810 |
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