SpineFrontier, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1664-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be used with a surgical system. Case and caddy components are used to contain implants intended for intervertebral body fusion and fixation of the spine.

Product Classification:

Class II

Date Initiated: May 17, 2013

Date Posted: July 10, 2013

Recall Number: Z-1664-2013

Event ID: 65432

Reason for Recall:

The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

Status: Terminated

Product Quantity: 12

Code Information:

Lot/Serial Numbers: 7201.007 and 7201.007-1

Distribution Pattern:

USA Nationwide including the states of: FL, CO, Wash DC, VA, KS, TX, OH, TN, OK, CA, IL, MO, and MN.

Voluntary or Mandated:

Voluntary: Firm initiated