Biomet Spine, LLC recalls

13 recalls on record · latest: February 12, 2016

Official U.S. recall history for Biomet Spine, LLC, compiled from official government records.

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Biomet Spine product recalled over labeling errors

February 12, 2016 · Medical device recalls Moderate risk Zimmer Biomet Spine initiated a recall of certain Solitaire Ti Spacers because…

Biomet Spine, LLC recalls MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Anterior Cervical Plate…

September 29, 2015 · Medical device recalls Moderate risk The packaging of 4.5 mm diameter MaxAn screws identifies/labels the screws as 4…

Biomet Parsippany recalled over labeling errors

August 5, 2015 · Medical device recalls Moderate risk Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

Biomet Spine, LLC recalls Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft, Model Numbers 14-525050 and 14-525057, reusab…

July 22, 2015 · Medical device recalls Moderate risk Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible and i…

Biomet Spine, LLC recalls Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provides posterior fixation in the non-cer…

March 12, 2015 · Medical device recalls Moderate risk Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque Limit…

Biomet Spine, LLC recalls Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct Usage: Designed to facilitate reconstruction of…

March 12, 2015 · Medical device recalls Moderate risk Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque Limit…

Polaris 4 recalled over sterility concerns

March 12, 2015 · Medical device recalls Moderate risk Multiaxial screws may not meet internal requirements related to fatigue strengt…

Biomet Spine, LLC recalls Timberline Anchored Lateral Fixed Retractable Sleeve Model No. 8630-0205. Timberline Anchored Lateral Fixed Retractable…

August 22, 2013 · Medical device recalls Moderate risk The inner diameter of the Sleeve shaft is undersized, resulting in interference…

Biomet Spine, LLC recalls Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. Timberline Anchored Lateral Retra…

August 22, 2013 · Medical device recalls Moderate risk The outer diameter of the Drill shaft is oversized; thereby, resulting in inter…

Biomet Spine, LLC recalls Timberline Anchored Lateral Variable Retractable Sleeve LITPCR8600-2101-07, Model No. 86300204 Timberline Anchored Lat…

August 22, 2013 · Medical device recalls Moderate risk The inner diameter of the Sleeve shaft is undersized, resulting in interference…

Set Screw 5 recalled over sterility concerns

November 30, 2012 · Medical device recalls Moderate risk Biomet Spine LLC is recalling the Set Screw 5.5 mm Rod due to the set screw bei…

Biomet Spine, LLC recalls Timberline Cranial Caudal and Posterior Blades, 40 - 180mm Model # 8734-2XXX, 8734-5XXX is a reusable device provided w…

February 22, 2012 · Medical device recalls Moderate risk Biomet Spine, LLC is recalling the Timberline Cranial Caudal and Posterior Blad…

Biomet Spine, LLC recalls Telluride Percutaneous Rod Inserter Long, Model #7706-1904. The Inserter is a reusable device provided within an alumin…

December 19, 2011 · Medical device recalls Moderate risk The Telluride Percutaneous Rod Inserter Long does not contain a feature that lo…