Device recall
Z-0994-2007: Vortech Graft Preparation System, sterile, single use, disposable, Distributed…
FDA device recall · Class III · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0994-2007 |
|---|---|
| Recall event | 38116 |
| Product | Vortech Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300V. (Not sold in the United States). |
| Product code | FMF |
| Recalling firm | Biomet, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 5, 2007 |
| FEI number | 1825034 |
At a glance
- None 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