Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case contained a bracket with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact SpineFrontier, Inc. directly.
Affected Products
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.
Quantity: 12
Why Was This Recalled?
The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About SpineFrontier, Inc.
SpineFrontier, Inc. has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report