K2M, Inc recalls

39 recalls on record · latest: June 13, 2022

Official U.S. recall history for K2M, Inc, compiled from official government records.

Get recall alerts

Free email alert whenever K2M, Inc has a new recall — straight from official government data. Unsubscribe anytime.

K2M, Inc. recalls Yukon Straight Rod 4.0 x120mm; Cat# 7601-540120. Used to provide immobilization and stabilization of spinal segments.

June 13, 2022 · Medical device recalls Moderate risk Some of the rods in this lot were observed to have discoloration, later confirm…

K2M, Inc recalls Everest MI XT Inner Dilator, Catalog Number 5101-90167

January 13, 2022 · Medical device recalls Moderate risk Stryker received two (2) complaints for units from specific lots of Inner and O…

K2M, Inc recalls Everest MI XT Outer Dilator, Catalog Number 5101-90168

January 13, 2022 · Medical device recalls Moderate risk Stryker received two (2) complaints for units from specific lots of Inner and O…

K2M, Inc recalls Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068

September 8, 2021 · Medical device recalls Moderate risk Units may arrive with missing pins and/or in a state in disassembly. Pins dislo…

K2M product recalled over labeling errors

May 7, 2021 · Medical device recalls Moderate risk Mislabeled product labeling references incorrect length or height, or length an…

K2M product recalled over labeling errors

May 7, 2021 · Medical device recalls Moderate risk Mislabeled product labeling references incorrect length or height, or length an…

K2M product recalled over labeling errors

May 7, 2021 · Medical device recalls Moderate risk Mislabeled product labeling references incorrect length or height, or length an…

K2M, Inc recalls Chesapeake Cervical-Ti 10mm Drill Guide Inserter- a multi-screw construct providing stability to the anterior column (c…

March 16, 2021 · Medical device recalls Moderate risk Interference condition between the 10mm Drill Guide Inserter and the inner shaf…

K2M, Inc recalls Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026), component of YUKON Spinal System

December 14, 2020 · Medical device recalls Moderate risk The Yukon polyaxial screw used in the Yukon Spinal System was incorrectly laser…

K2M, Inc recalls Everest MI XT Tab Removal Tool (i.e. All-In-One Tab Removal Tool)-used to break the tab off the Everest XT screw by roc…

November 4, 2020 · Medical device recalls Moderate risk All-in-One Tab Removal Tool may cause cracking and/or separating at the threade…

K2M, Inc recalls Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment Tube (the Alignment…

November 3, 2020 · Medical device recalls Moderate risk Shafts do not pass through the inner cannula of the Anti-Torque Alignment Tube…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

K2M product recalled over sterility concerns

April 13, 2020 · Medical device recalls Moderate risk The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two piec…

Fenestrated Taps 4 recalled over labeling errors

April 18, 2019 · Medical device recalls Moderate risk The products are mislabeled.

K2M product recalled over labeling errors

April 18, 2019 · Medical device recalls Moderate risk The products are mislabeled.

K2M, Inc recalls YUKON Polyaxial Screws (3.5 X 12 mm, Owning Site: Leesburg USA 3.5 X 14 mm, 3.5 X 32 mm, 3.5 X 34 mm, 3.5 X 38 mm, 3.5…

July 24, 2018 · Medical device recalls Moderate risk Screws had a manufacturing error that could prevent the screw from mating with…

K2M, Inc recalls K2M Special Connector Instruments (Special Connector, Special Adaptor, and Quick Adaptor) Product Usage: Special Connec…

December 2, 2016 · Medical device recalls Moderate risk Instruments were developed without adequate consideration given to the need for…