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Biomet Spine, LLC recalls Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. Timberline Anchored Lateral Re
Recalled January 21, 2015 · FDA recall Z-0982-2015 · Biomet Spine
Hazard
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. · FDA Class II
Units
15
Sold at
Distributed in PR and the states of NY, AZ, TN, TX, and CA.
Description
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.
Product
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.
Manufacturer(s)
Biomet Spine, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →