Device recall
Z-0952-04: BioPince Full Core Biopsy Instrument packed in aTyvek/plastic blister pack which…
FDA device recall · Class II · Medical Device Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0952-04 |
|---|---|
| Recall event | 29023 |
| Product | BioPince Full Core Biopsy Instrument packed in aTyvek/plastic blister pack which is labeled as previously stated and also in a cardboard shelf carton labeled as MDTECH Gainesville, Florida 32608 BioPince FULL CORE BIOPSY INSTRUMENT ga. cm REF: Lot |
| Product code | GAA |
| Recalling firm | Medical Device Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 7, 2012 |
| 510(k) numbers | K904987 |
| FEI number | 1036710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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