Device recall
Z-0519-2007: The recalled product is the Large grid biopsy plate, part #2414797. The biopsy…
FDA device recall · Class II · USA Instruments Incorporated
Key facts
| Recall number (Z-number) | Z-0519-2007 |
|---|---|
| Recall event | 37263 |
| Product | The recalled product is the Large grid biopsy plate, part #2414797. The biopsy plate is labeled in part: Large Grid Biopsy Plate, part 2414797, For Use with the Liberty 9000 8-Channel Breast Coil, USA Instruments, Inc., Aurora, OH, sterile. The breast biopsy plate is used with OEM coils (coils… |
| 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