Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a Recalled by Lucero Medical LLC Due to The firm voluntarily recalled the device after they...
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 Lucero Medical LLC directly.
Affected Products
Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a vertebral body replacement system intended for use in the thoracic and lumbar spine (T1-S1) to replace a collapsed, damaged or unstable vertebral body due to tumor or trauma/fracture. The device is intended for use with either allograft or autograft. The device may be used with a cleared supplemental fixation system based on surgeon discretion and preference.
Quantity: 169
Why Was This Recalled?
The firm voluntarily recalled the device after they discovered that the sterilization recommendations on the product insert did not pass sterilization validation.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lucero Medical LLC
Lucero 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