Spinal Elements, Inc: Medical Device Recalls in 2015

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Spinal Elements, Inc in 2015. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.
Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprised of a variety of screws, hooks, rods, connectors, and staples that are used for attachment to the non-cervical spine. Rods span the distance between screws and hooks and achieve fixation by the mechanical joining of the rods with the screws or hooks. Lordosed rods are pre-curved to better fit the patient anatomy.