Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces voluntary recall of Durango...
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 Biomet Spine LLC. directly.
Affected Products
LANX, REF, PCR8XXX-XXX, LOT, RXONLY. Packaged within aluminum sterilization case. Product Usage: The Durango implant is intended for spinal fusion procedures to be used with autogenous bone graft in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous spinal levels from L2S1.
Quantity: 120
Why Was This Recalled?
Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate due to the set screw component potentially becoming dislodged from the plate assembly.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Biomet Spine LLC.
Biomet Spine 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