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Ebi, Llc recalls Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number 14-500178. The Polaris Spinal System is a non-ce

Recalled March 27, 2013 · FDA recall Z-0954-2013 · Ebi

Hazard
Increased risk of failure at the driver tip during screw insertion or removal. · FDA Class II
Units
59 units.
Sold at
Nationwide Distribution including the states of AL, IN, MO, NE TN and TX.

Description

Increased risk of failure at the driver tip during screw insertion or removal.

Product
Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number 14-500178. The Polaris Spinal System is a non-cervical, pedicle screw spinal fixation device.
Manufacturer(s)
Ebi, Llc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Ebi, Llc recalls Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number 14-500178. The Polaris Spinal System is a non-ce | RecallWatchUSA