Device recall
Z-2335-2021: AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
FDA device recall · Class II · BioMimetic Therapeutics, LLC
Key facts
| Recall number (Z-number) | Z-2335-2021 |
|---|---|
| Recall event | 88395 |
| Product | AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343 |
| Product code | NOX |
| Recalling firm | BioMimetic Therapeutics, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 4, 2024 |
| PMA numbers | P100006 |
| FEI number | 3003897776 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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