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SpineFrontier, Inc. recalls BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be
Recalled July 10, 2013 · FDA recall Z-1664-2013 · SpineFrontier
Hazard
The S-LIFT Instrument Case contained a bracket with peeling nylon coating. · FDA Class II
Units
12
Sold at
USA Nationwide including the states of: FL, CO, Wash DC, VA, KS, TX, OH, TN, OK, CA, IL, MO, and MN.
Description
The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Product
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.
Manufacturer(s)
SpineFrontier, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →