BEUDAMED
    117 results · 21ms · Sources: EU EUDAMED, US FDA

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    LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 5, RIGHT, REF 71426005, QTY 1, Smith & Nephew, knee prosthesis Usage:orthopedic.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code JWH·November 4, 2014

    LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 6, LEFT, REF 71426006, QTY 1, Smith & Nephew, knee prosthesis Usage:orthopedic.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code JWH·November 4, 2014

    LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT, SIZE 4, LEFT, REF 71425004, QTY 1, Smith & Nephew, knee prosthesis Usage:orthopedic.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code JWH·November 4, 2014

    smith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STRAIGHT PLATE, 8 HOLE VLP(R) MIN-MOD, REF 74442024, QTY: (1), STERILE R Bone plates and bone screws from the Smith & Nephew Variable-Angle Locking Mini-Fragment Plating System (VLP MINI-MOD) are intended for use in internal fixation of small bones and small bone fragments and non-load bearing stabilization and reduction of bone fragments in long bones.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HRS·December 11, 2017

    smith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STOUT STRAIGHT PLATE, 8 HOLE VLP(R) MIN-MOD, REF 74442030, QTY: (1), STERILE R Bone plates and bone screws from the Smith & Nephew Variable-Angle Locking Mini-Fragment Plating System (VLP MINI-MOD) are intended for use in internal fixation of small bones and small bone fragments and non-load bearing stabilization and reduction of bone fragments in long bones.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HRS·December 11, 2017

    Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: 7211015 Used during ligament reconstruction.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code MAI·July 19, 2016

    Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code NBH·January 11, 2016

    ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended for Meniscal Repair.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code GAT·April 30, 2015

    Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code MBL·January 23, 2014

    REFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,. Memphis, TN 38116

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code JDI·November 16, 2016

    12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW STEMS AND 12/14 FEMORAL COMPONENTS ONLY CO-CR, REF 71352112, Smith & Nephew, Inc. Memphis, TN 38116 USA. USE WITH SMITH & NEPHEW STEMS AND 12/14 FEMORAL COMPONENTS.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code MEH·August 22, 2012

    GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 5, LEFT, QTY: (1), REF 71420168. Product Usage: orthopaedic

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code JWH·October 7, 2013

    GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188. Product Usage: orthopaedic

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code JWH·October 7, 2013

    NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusable instrument designed to, when used as instructed, provide the required bone pin spacing for the Navio bone clamps and potentially reduce the amount of patient tissue affected when placing the bone pins.

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code OLO·February 27, 2020