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All product recalls associated with Alphatec Spine, Inc. 1950 Camino Vida Roble.
Total Recalls
5
Past Year
0
Class I (Serious)
0
Most Recent
Dec 2024
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Complaints have been received regarding post-operative implant collapse.
Due to reports of intraoperative graft bolt implantation breakages.
Awl instrument adjustable drill button assembly assembled in the incorrect orientation, preventing locking feature from engaging with shaft at the desired set point; instruments lack ability to control awl depth by means of adjustable shaft advancement stop, which may lead to over insertion, dural tear, vascular/neurologic injury, adjacent tissue damage, increased operative time, revision surgery.