Device recall
Z-0618-2008: InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers…
FDA device recall · Class III · Interpore Cross International Inc
Key facts
| Recall number (Z-number) | Z-0618-2008 |
|---|---|
| Recall event | 45469 |
| Product | InterGro PLUS; DBM in a Lipid Carrier with Calcium Granules; Model Numbers: DBM002, DBM005, DBM010, DBMW05 & DBMW10, Interpore Cross International, a Biomet company (lnterGro DBM products contain human tissue (allograft bone) and are intended for transplantation) |
| Product code | MQV |
| Recalling firm | Interpore Cross International Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 25, 2008 |
| 510(k) numbers | K031399 |
| FEI number | 1000160576 |
At a glance
- 1–9 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