Device recall
Z-1562-2014: AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for…
FDA device recall · Class II · AlloSource, Inc.
Key facts
| Recall number (Z-number) | Z-1562-2014 |
|---|---|
| Recall event | 67986 |
| Product | AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as filler for gaps or voids that are not intrinsic to the stability of the bony structure. AlloFuse is indicated to be packed gently into bony gaps in the skeletal system as a bone graft extender. |
| Product code | MQV |
| Recalling firm | AlloSource, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2014 |
| 510(k) numbers | K071849 |
| FEI number | 3000215346 |
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