Device recall
Z-2264-2014: All brochures printed before November 20, 2013 for the HyperBlue 1530 medical…
FDA device recall · Class II · Hyperion Medical
Key facts
| Recall number (Z-number) | Z-2264-2014 |
|---|---|
| Recall event | 67814 |
| Product | All brochures printed before November 20, 2013 for the HyperBlue 1530 medical laser, including the product brochure and the online information regarding the product at www.hyperionMed.com before December 3, 2013. |
| Product code | PDZ |
| Recalling firm | Hyperion Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2015 |
| FEI number | 3007674911 |
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