Device recall
Z-1207-2009: Biomet Marrowstim Concentration Kit w/single Disposable Separator, Bone Marrow…
FDA device recall · Class III · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1207-2009 |
|---|---|
| Recall event | 51316 |
| Product | Biomet Marrowstim Concentration Kit w/single Disposable Separator, Bone Marrow Needle, and 30 ml ACD-A. For use with BBI centrifuges only, sterile, Biomet Biologics, Warsaw, IN; REF 800-0611A and 800-0613A. The device is used for the rapid preparation of platelet-poor-plasma and platelet concentrate… |
| Product code | JQC |
| Recalling firm | Biomet, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 7, 2009 |
| 510(k) numbers | K071934 |
| FEI number | 1825034 |
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