Device recall
Z-0518-2013: Quasar MD is an infrared LED lamp that is labeled in part: "***QUASAR…
FDA device recall · Class II · Quasar Bio-Tech, Inc. dba Silver Bay LLC
Key facts
| Recall number (Z-number) | Z-0518-2013 |
|---|---|
| Recall event | 63530 |
| Product | Quasar MD is an infrared LED lamp that is labeled in part: "***QUASAR MD***Bringing the Spa Home***Radiant and Youthful Skin***QUASAR MD INCLUDES***QUASAR MD***USER MANUAL***12 VOLT POWER SUPPLY***1 OZ PURE SILK SERUM***Made in the USA.***Five year warranty***" The product emits energy in the near… |
| Product code | ILY |
| Recalling firm | Quasar Bio-Tech, Inc. dba Silver Bay LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 21, 2013 |
| 510(k) numbers | K051046 |
| FEI number | 3006182559 |
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