Device recall
Z-0025-2011: Tru-Core II Disposable Automatic Biopsy Instrument and Tru-Core II URO…
FDA device recall · Class II · Medical Device Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0025-2011 |
|---|---|
| Recall event | 56767 |
| Product | Tru-Core II Disposable Automatic Biopsy Instrument and Tru-Core II URO Disposable Automatic Biopsy Instrument. The Tru-Core Disposable Automatic Biopsy Instrument is used to obtain multiple core samples from soft tissue such as liver, kidney, prostate, breast, ect. The recalling lot's for the… |
| Product code | MJG |
| Recalling firm | Medical Device Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2011 |
| 510(k) numbers | K982960 |
| FEI number | 1036710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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