Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic implant) Recalled by 4-Web Inc. Due to Mislabeling
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 4-Web Inc. directly.
Affected Products
ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic implant) Large, 12 degrees lordosis, 12 mm height and ASTS-LG0612: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic implant) Large, 6 degrees lordosis, 12 mm height
Quantity: 35 units
Why Was This Recalled?
Product is mislabeled.
Where Was This Sold?
This product was distributed to 6 states: CA, IL, MD, MT, TX, DC
About 4-Web Inc.
4-Web Inc. 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