Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Anchored Lateral Retractable Drill Recalled by Biomet Spine, LLC Due to The outer diameter of the Drill shaft is...
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
Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. Timberline Anchored Lateral Retractable Drills are used with the Timberline MPF System to establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae.
Quantity: 15
Why Was This Recalled?
The outer diameter of the Drill shaft is oversized; thereby, resulting in interference fit when inserting the Drill into the Fixed or Variable Sleeve Assembly.
Where Was This Sold?
This product was distributed to 5 states: AZ, CA, NY, TN, TX
About Biomet Spine, LLC
Biomet Spine, LLC has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report