Device recall
Z-0935-03: Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product…
FDA device recall · Class II · Sanarus Medical Inc
Key facts
| Recall number (Z-number) | Z-0935-03 |
|---|---|
| Recall event | 26324 |
| Product | Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product Code: CD-0500 (single Device); CD-1000 (5 pack) |
| Product code | KNW |
| Recalling firm | Sanarus Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 15, 2003 |
| 510(k) numbers | K022879 |
| FEI number | 3003515897 |
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