Device recall
Z-0519-2013: Quasar Power Pack contains a Baby Quasar and a Baby Blue. The Baby Quasar is an…
FDA device recall · Class II · Quasar Bio-Tech, Inc. dba Silver Bay LLC
Key facts
| Recall number (Z-number) | Z-0519-2013 |
|---|---|
| Recall event | 63530 |
| Product | Quasar Power Pack contains a Baby Quasar and a Baby Blue. The Baby Quasar is an infrared LED lamp. The Baby Blue uses blue LED light to be used in combination with the Baby Quasar to treat acne. The Quasar Power Pack is labeled in part: "***BABY QUASAR & BABY BLUE***QUASAR POWERPACK***FOR YOUTHFUL… |
| 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