Device recall
Z-0123-2014: Globus Medical MicroFuse Putty, 2.5cc and 10cc. Product Usage: MicroFuse Bone…
FDA device recall · Class II · Globus Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0123-2014 |
|---|---|
| Recall event | 66266 |
| Product | Globus Medical MicroFuse Putty, 2.5cc and 10cc. Product Usage: MicroFuse Bone Void Filler is indicated only for bony voids or gaps that are not intrinsic to the stability of the bony structure. MicroFuse Bone Void Filleris a bone graft extender to be used with autogenous bone marrow aspirate or… |
| Product code | MQV |
| Recalling firm | Globus Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 14, 2014 |
| 510(k) numbers | K102392 |
| FEI number | 3004142400 |
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