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Biomet Spine, Llc Recalls

8 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Biomet Spine, Llc.

8Total Recalls
0Critical
3,287Units Affected
Sep 29, 2015Most Recent
All Recalls

Every Biomet Spine, Llc Recall

Sorted by most recent. Click any recall for full details.

8 recalls
High RiskFDA
Biomet Spine, Llc
MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Anterior Cervical Plate System is a decom...
Medical Devices·17 affected·Sep 29, 2015
High RiskFDA
Biomet Spine, Llc
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Medical Devices·7 affected·Aug 5, 2015
High RiskFDA
Biomet Spine, Llc
Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provides posterior fixation in the non-cervical spine ...
Medical Devices·874 affected·Mar 12, 2015
High RiskFDA
Biomet Spine, Llc
Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct Usage: Designed to facilitate reconstruction of the cervical a...
Medical Devices·148 affected·Mar 12, 2015
High RiskFDA
Biomet Spine, Llc
Timberline Anchored Lateral Fixed Retractable Sleeve Model No. 8630-0205. Timberline Anchored Lateral Fixed Retractable Sleeves are used...
Surgical Devices·14 affected·Aug 22, 2013
High RiskFDA
Biomet Spine, Llc
Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. Timberline Anchored Lateral Retractable Drills ...
Medical Devices·15 affected·Aug 22, 2013
High RiskFDA
Biomet Spine, Llc
Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: The titanium alloy set screw is used to seat a 5.5 mm titanium alloy, commerci...
Medical Implants·1,999 affected·Nov 30, 2012
High RiskFDA
Biomet Spine, Llc
Timberline Cranial Caudal and Posterior Blades, 40 - 180mm Model # 8734-2XXX, 8734-5XXX is a reusable device provided within an aluminum ...
Medical Devices·213 affected·Feb 22, 2012