FDA Device recall Z-1721-2015
Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25
- FDA Device
- Class II
- terminated
- Published 2015-06-17
On 2015-06-17 the FDA classified a Class II recall of Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25 by Vilex In Tennessee, citing incidence of breakage is higher than expected.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1721-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-22 |
| Published | 2015-06-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Vilex In Tennessee |
| Distribution | MD, MS, PA, TX |
Product
Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
Reason
Incidence of breakage is higher than expected.
Identifiers
| code_info | all codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1721-2015%22
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