Device recall
Z-0699-06: Osteofil Allograft, 5cc. Product is labeled in part: ''***Processed at…
FDA device recall · Class III · Regeneration Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0699-06 |
|---|---|
| Recall event | 34367 |
| Product | Osteofil Allograft, 5cc. Product is labeled in part: ''***Processed at: Regeneration TECHNOLOGIES, INC. Alachua, Florida USA***SINGLE PATIENT USE ONLY***''. |
| Product code | MQV |
| Recalling firm | Regeneration Technologies, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 7, 2012 |
| FEI number | 3002719998 |
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