Device recall
Z-2181-2014: Luma Wrap Phototherapy Swaddler is designed to provide centered and comfortable…
FDA device recall · Class II · Beevers Manufacturing & Supply, Inc.
Key facts
| Recall number (Z-number) | Z-2181-2014 |
|---|---|
| Recall event | 68803 |
| Product | Luma Wrap Phototherapy Swaddler is designed to provide centered and comfortable boundaries as a benefit for restive babies in the Neonatal Intensive Care Unit. |
| Product code | PDH |
| Recalling firm | Beevers Manufacturing & Supply, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2015 |
| FEI number | 3023468 |
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