Device recall
Z-2832-2018: TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin for…
FDA device recall · Class II · Beekley Corporation
Key facts
| Recall number (Z-number) | Z-2832-2018 |
|---|---|
| Recall event | 80558 |
| Product | TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin for marking and identifying moles in mammography. |
| Product code | JAC |
| Recalling firm | Beekley Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 13, 2018 |
| 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