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Vilex In Tennessee Inc recalls Vilex, Inc., FUZE 10.0 mm x 250 mm, Product # FZ100-250T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
Recalled June 17, 2015 · FDA recall Z-1723-2015 · Vilex In Tennessee
Hazard
Incidence of breakage is higher than expected. · FDA Class II
Units
4 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 250 mm, Product # FZ100-250T-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 →