FDA Device recall Z-2335-2021
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
- FDA Device
- Class II
- terminated
- Published 2021-09-01
On 2021-09-01 the FDA classified a Class II recall of AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343 by Biomimetic Therapeutics, citing the kit contains the wrong vial tray in the package.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2335-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-07-23 |
| Published | 2021-09-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Biomimetic Therapeutics |
| Distribution | US |
Product
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Reason
The kit contains the wrong vial tray in the package.
Identifiers
| code_info | Model Number K30003010, Lot 1706343 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2335-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.