592 results
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12ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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METRx II Tube, 20mm x 6cm stainless steel tubular retractor, Part No. 9569723
FDA Recall
Terminated
·Medtronic Sofamor Danek Instrument Manufacturing·Product code LXH·January 25, 2006
METRx II Tube, 14mm x 5cm stainless steel tubular retractor, Part No. 9569662
FDA Recall
Terminated
·Medtronic Sofamor Danek Instrument Manufacturing·Product code LXH·January 25, 2006
METRx II Tube, 18mm x 4cm stainless steel tubular retractor, Part No. 9569681
FDA Recall
Terminated
·Medtronic Sofamor Danek Instrument Manufacturing·Product code LXH·January 25, 2006
Biomet Vanguard Lock-On Femoral Impactor, Biomet Orthopedics. Warsaw. IN; REF 32-486206. Non-powered, hand-held device intended for medical purposes for use with other devices in orthopedic surgery; impactor.
FDA Recall
Terminated
·Biomet, Inc.·Product code LXH·December 1, 2009
Byrd Screw, 2.0X6MM SD, Model Number: 01-0264 Product labeling reads in part as follows: REF: 01-0264, QTY,UOM 00001, BYRD SCREW, 2 OX6MM SELF-DRILLING, 12CM, (4-3/4) (L), STAINLESS STEEL, LOT 999999, (01) 00841036007157(10)999999(13)090201(30)13, 2009-02, ***NON-STERILE PRODUCT***DD 14 03 1, BIOMET MICROFIXATION, INC., 150 TRADEPORT DRIVE, JACKSONVILLE, FL 32218 USA Instrument used to pull up the broken bone, so it is flush and can be plated fixated. The Byrd screw is then removed.
FDA Recall
Terminated
·Biomet Microfixation, Inc.·Product code LXH·February 19, 2009
"***BIOMET MICROFIXATION***CENTER DRIVE STAINLESS STEEL***2.0MM SYSTEM SCREWDRIVER BLADE***Non-Sterile Product***BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com***" Blade used to implant screws.
FDA Recall
Terminated
·Biomet Microfixation, Inc.·Product code LXH·March 15, 2010
Specialist 2 IM Rod, Non-Sterile and associated Surgical Techniques: Sigma HP Instruments Classic Surgical Technique,0612-89-510 Sigma HP Instruments Balanced Surgical Technique, 0612-88-510 Sigma HP Instruments Fixed Reference Surgical Technique, 0612-87-510 PFC Sigma Knee Systems Primary Cruciate-Retaining & Cruciate-Substituting Procedure Surgical Technique,SP2-007 Product Usage: The SP2 IM Rod is used in both primary and revision Sigma knee procedures to align the femoral locating device and distal femoral cutting block. It is also used with the IM tibial resection. This rod is included in both the SP2 and HP instrument kits.
FDA Recall
Terminated
·DePuy Orthopaedics, Inc.·Product code LXH·February 5, 2013
Cypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System is a non-cervical spinal fixation device. 1)Screw Tower - REF 14-501660 2) Rod Reduce - REF 14-501661 3) Counter Torque - REF 14-501662
FDA Recall
Terminated
·Ebi, Llc·Product code LXH·August 13, 2013
REF 8788, 8mm C-REAMER, CANNULATED, STERILE, Rx ONLY. CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA. Intended for use in Arthroscopic knee procedures.
FDA Recall
Terminated
·Linvatec Corp. dba ConMed Linvatec·Product code LXH·January 28, 2010
Zimmer ITST" INTERTROCHANTERIC/SUBTROCHANTERIC FIXATION LOCKING BOLT EXTRACTOR - NONSTERILE Zimmer, Warsaw, IN 46580, U.S.A. The ITST Intertrochanteric/Subtrochanteric Fixation Locking Bolt Extractor instrument is a reusable surgical instrument used to separate the femoral nail from the locking bolt after nail implantation/fixation in trauma surgeries
FDA Recall
Terminated
·Zimmer Inc.·Product code LXH·July 5, 2010
MIKA Speedblock, Size 8-12. The MIKA Speedblock is placed on the distal femur as a guide for making the anterior, posterior and both chamfer cuts.
FDA Recall
Terminated
·Product code LXH·April 26, 2010
NexGen Complete Knee Solution Rotating Hinge Knee tibial broach impactor, Catalog # 00-5881-080-00, Zimmer Inc., Warsaw, IN.
FDA Recall
Terminated
·Zimmer Inc.·Product code LXH·April 16, 2010
Scorpio Fixed Femoral A/P Sizing Guide; non-sterile instruments; Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430; A subsidiary of Stryker Corporation The A/P sizer is designed to set the desired external rotation and to provide adjustment of the anterior/posterior position when needed.
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code LXH·September 27, 2010
Vl DBL OFFST WI LRG STPL, RT Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
VER2 HANDLE, PIN REWORK, LT Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
VI DBL OFFST W/ LRG STPL, LT Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
Double Offset Rasp Handle, Left Hand Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
VER2 D8L OFFSET RASP HANDLE, RT Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
Specialty Aria Inserter, REF IS3021ARI, Non-Sterile, This instrument is part of the Aria product brand. It is used for Implant insertion into the disc space. The Aria Inserter PEEK Spacer System offers implants that are interbody fusion devices intended for use as an aid in spinal fixation. These hollow implants are offered in a variety of lengths, heights, and lordotic angles designed to adapt to different patient anatomies. They have serrations on the superior and inferior surfaces designed for multidirectional fixation, ergonomically shaped anterior edges, and flat posterior edges. This device does not sustain or support life.
FDA Recall
Terminated
·Stryker Spine·Product code LXH·July 7, 2014
Zimmer Minimally Invasive Solutions Technology, Offset Rasp Handle, Left, 45 degrees, non-sterile; REF/Catalog #: 7712-35-01, Zimmer U.K. Ltd., SN3, 4FP, UK
FDA Recall
Terminated
·Zimmer Inc.·Product code LXH·June 28, 2007