Drug recall
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
FDA recall event 88395 · Class II · BioMimetic Therapeutics, LLC
Key facts
| Event ID | 88395 |
|---|---|
| Recall numbers | Z-2335-2021 |
| Recalling firm | BioMimetic Therapeutics, LLC |
| Product type | Devices |
| Products | AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The kit contains the wrong vial tray in the package. |
| Initiation date | Jul 23, 2021 |
| Report date | Sep 1, 2021 |
| Termination date | Sep 4, 2024 |
| City | Franklin |
| State | TN |
| Country | United States |
| FEI number | 3003897776 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: