AUGMENT Injectable Kit — Class II medical device recall Z-2335-2021
Terminated recall by BioMimetic Therapeutics, LLC, reported 2021-09-01, distributed nationwide. The kit contains the wrong vial tray in the package.
| Recall number | Z-2335-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | BioMimetic Therapeutics, LLC, Franklin, TN, United States |
| Recall initiated | 2021-07-23 |
| Classified | 2021-08-23 |
| Reported by FDA | 2021-09-01 |
| Terminated | 2024-09-04 |
| Distributed | Nationwide (US) |
| Quantity | 499 units |
| Lot numbers | 1706343 |
| Model numbers | K30003010 |
Product
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Reason for recall
The kit contains the wrong vial tray in the package.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2335-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.