Device recall
Z-0505-2007: LATERAL BIOPSY PLATE - For use with the Liberty 9000, 8-Channel Breast Coil. The…
FDA device recall · Class II · USA Instruments Incorporated
Key facts
| Recall number (Z-number) | Z-0505-2007 |
|---|---|
| Recall event | 36866 |
| Product | LATERAL BIOPSY PLATE - For use with the Liberty 9000, 8-Channel Breast Coil. The Lateral Biopsy plate is sent to customers in the following configurations: 1) The plate is purchased in sets of 5 as part number E8800BG 8 Channel Breast Biopsy Lateral Grids (pack of 5 grids) or 2) the plate is… |
| Product code | LNH |
| Recalling firm | USA Instruments Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2012 |
| 510(k) numbers | K041695, K052585 |
| FEI number | 3005214683 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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