Device recall
Z-1138-2013: OsteoSelect DBM Putty Product Usage: Orthopedic bone filler
FDA device recall · Class II · Bacterin International, Inc.
Key facts
| Recall number (Z-number) | Z-1138-2013 |
|---|---|
| Recall event | 64486 |
| Product | OsteoSelect DBM Putty Product Usage: Orthopedic bone filler |
| Product code | MBP |
| Recalling firm | Bacterin International, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 1, 2013 |
| 510(k) numbers | K091321 |
| FEI number | 3005031160 |
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