Device recall
Z-0825-2008: OsteoStim Cervical Allograft (Lordotic Cervical Spacer) H. 7mm; W. 14mm; L…
FDA device recall · Class III · EBI, L.P.
Key facts
| Recall number (Z-number) | Z-0825-2008 |
|---|---|
| Recall event | 45502 |
| Product | OsteoStim Cervical Allograft (Lordotic Cervical Spacer) H. 7mm; W. 14mm; L. 10mm., Catalog Number: 45-5537 and Catalog Number : LGAL906, Distributed by EBI. (dba Biomet Spine, Biomet Trauma, Biomet Bracing, Biomet Osteobiologics) Parsippany, New Jersey 07054 |
| Product code | MQV |
| Recalling firm | EBI, L.P. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 15, 2008 |
| FEI number | 2242816 |
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