Device recall
Z-2112-2012: Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for…
FDA device recall · Class II · Beekley Corporation
Key facts
| Recall number (Z-number) | Z-2112-2012 |
|---|---|
| Recall event | 62526 |
| Product | Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain |
| Product code | JAC |
| Recalling firm | Beekley Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 9, 2013 |
| FEI number | 3000204334 |
At a glance
- None 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