Home / Recalls / Medical Devices
SPINEART SA recalls Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Recalled December 4, 2019 · FDA recall Z-0546-2020 · SPINEART SA
Hazard
Inner blister pack label is incorrect and does not match the correct external box label. · FDA Class III
Units
14 pieces distribtued to 1 US Distributor
Sold at
US: CA OUS: Unknowns
Description
Inner blister pack label is incorrect and does not match the correct external box label.
Product
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Manufacturer(s)
SPINEART SA
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →