Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Timberline Anchored Lateral Variable Retractable Sleeve LITPCR8600-2101-07 Recalled by Biomet Spine, LLC Due to The inner diameter of the Sleeve 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
Timberline Anchored Lateral Variable Retractable Sleeve LITPCR8600-2101-07, Model No. 86300204 Timberline Anchored Lateral Variable Retractable Sleeves (the Sleeves) are used with the Timberline MPF System to help establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae.
Quantity: 12 units
Why Was This Recalled?
The inner diameter of the Sleeve shaft is undersized, resulting in interference fit when inserting the Anchored Lateral Straight Retractable Awl or the Anchored Lateral Straight Retractable Drill into the Sleeve shaft.
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