Device recall
Z-0329-2011: Titan XL Handpiece Infrared Therapeutic Heating Lamp, Manufactured by Cutera…
FDA device recall · Class II · Cutera Inc
Key facts
| Recall number (Z-number) | Z-0329-2011 |
|---|---|
| Recall event | 55840 |
| Product | Titan XL Handpiece Infrared Therapeutic Heating Lamp, Manufactured by Cutera Inc, Brisbane, CA Infrared therapeutic heating lamp, intended to emit energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and… |
| Product code | ILY |
| Recalling firm | Cutera Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 28, 2010 |
| 510(k) numbers | K042165 |
| FEI number | 3002900199 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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