FDAApril 22, 2015device
Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-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.
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