Device recall
Z-1787-2014: Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product…
FDA device recall · Class III · Beekley Corporation
Key facts
| Recall number (Z-number) | Z-1787-2014 |
|---|---|
| Recall event | 65483 |
| Product | Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography |
| Product code | MUE |
| Recalling firm | Beekley Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 16, 2014 |
| 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