Device recall
Z-2351-2008: InterGro DBM Demineralized Bone Matrix in a lipid carrier; Provided by: Lifelink…
FDA device recall · Class II · Michigan Orthopaedic Products, Inc.
Key facts
| Recall number (Z-number) | Z-2351-2008 |
|---|---|
| Recall event | 48189 |
| Product | InterGro DBM Demineralized Bone Matrix in a lipid carrier; Provided by: Lifelink Tissue Bank, Tampa, Florida, EBI A Biomet Company, Parsippany, New Jersey; REF DBM002. InterGro DBM product contain human tissue (allograft bpm) and are intended for transplantation. Products are to be used for filling… |
| Product code | MQV |
| Recalling firm | Michigan Orthopaedic Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 21, 2008 |
| FEI number | 3006213866 |
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