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Vilex In Tennessee Inc recalls Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
Recalled June 17, 2015 · FDA recall Z-1721-2015 · Vilex In Tennessee
Hazard
Incidence of breakage is higher than expected. · FDA Class II
Units
13 units
Sold at
Distributed in the states of MS, MD, PA, and TX.
Description
Incidence of breakage is higher than expected.
Product
Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
Manufacturer(s)
Vilex In Tennessee Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →