Device recall
Z-1808-2010: Harris Medical UV Lamp; the device does not have a label identifying the name…
FDA device recall · Class II · Harris Medical Resources
Key facts
| Recall number (Z-number) | Z-1808-2010 |
|---|---|
| Recall event | 55724 |
| Product | Harris Medical UV Lamp; the device does not have a label identifying the name and place of business or manufacturer, packer or distributor. It is packaged with a "Harris UV Lamp Training Manual" |
| Product code | MXG |
| Recalling firm | Harris Medical Resources |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2010 |
| FEI number | 3007232259 |
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