Device recall
Z-0517-2013: Baby Quasar (LAB-001-D, BQ101) and Baby Quasar Pink (LAB-046-A BQ101-P) are…
FDA device recall · Class II · Quasar Bio-Tech, Inc. dba Silver Bay LLC
Key facts
| Recall number (Z-number) | Z-0517-2013 |
|---|---|
| Recall event | 63530 |
| Product | Baby Quasar (LAB-001-D, BQ101) and Baby Quasar Pink (LAB-046-A BQ101-P) are infrared LED lamps that are labeled in part: "***BABY QUASAR***FOR YOUTHFUL RADIANT SKIN***Skin Rejuvenating System with Sequepulse***Manufactured by: Silver Bay, LLC; Made in the USA, with highest quality components and… |
| 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