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Amendia, Inc recalls Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicate
Recalled January 18, 2017 · FDA recall Z-0966-2017 · Amendia
Hazard
Absent tantalum market pin. · FDA Class II
Units
6 devices
Sold at
US Distribution to GA only.
Description
Absent tantalum market pin.
Product
Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying radicular symptoms at the one level from C2-T1.
Manufacturer(s)
Amendia, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →