The proximal opening of the inserts exhibit an out of specification condition which would prevent the crossbar plates from appropriately engaging with the insert.
XTANT MEDICAL
Class I - Dangerous
Cervical Implants contain a label that incorrectly identifies the grade of titanium used.
Class I - Dangerous
The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
The firm received one customer complaint concerning three OsteoSelect Demineralized Bone Matrix (DBM) devices which contained 5.0cc of putty, instead of 10.00cc of putty as labeled.
This recall has been initiated due to a change in packaging and sterilization method to address potential risks of compromised sterilization presented by the existing configuration.
The material type on the label may incorrectly state Ti6Al-4V ELI. The rods are composed of Cobalt Chromium.