Device recall
Z-0955-2025: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix…
FDA device recall · Class II · IsoTis OrthoBiologics, Inc.
Key facts
| Recall number (Z-number) | Z-0955-2025 |
|---|---|
| Recall event | 95981 |
| Product | OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix, OsteoSurge 100 Demineralized Bone Matrix, 10cc, REF 56300100. |
| Product code | MQV |
| Recalling firm | IsoTis OrthoBiologics, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K242273 |
| FEI number | 3001503333 |
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