FDAApril 22, 2015device
Vilex, Inc., FUZE 10.0 mm x 250 mm, Product # FZ100-250T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Incidence of breakage is higher than expected.
What to do
FDA enforcement status: Terminated
Brands named
vilex
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →