Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF) Recalled by Advanced Research Medical, LLC Due to Potential shearing of the disposable blade may occur...
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 Advanced Research Medical, LLC directly.
Affected Products
ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease
Quantity: 1150 units
Why Was This Recalled?
Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Advanced Research Medical, LLC
Advanced Research Medical, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report