Device recall
Z-1579-2014: BIOPSY NEEDLE KIT, 9733068, PASSIVE
FDA device recall · Class II · Medtronic Navigation, Inc.
Key facts
| Recall number (Z-number) | Z-1579-2014 |
|---|---|
| Recall event | 68145 |
| Product | BIOPSY NEEDLE KIT, 9733068, PASSIVE |
| Product code | HAW |
| Recalling firm | Medtronic Navigation, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 29, 2014 |
| 510(k) numbers | K001284, K012937, K990214 |
| FEI number | 1000517638 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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