325 results
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20ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.
FDA Enforcement
Class II
·Terminated·The Anspach Effort, Inc.·July 13, 2016
Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc. (El Dorado Hills, CA) & manufactured under Synvasive Technology, Inc. El Dorado Hills, CA Reciprocating saw blade: A sterile surgical saw blade used to resect damaged cartilage and/or bond in an orthopaedic reconstructive procedure such as a total knee replacement.
FDA Enforcement
Class II
·Terminated·Synvasive Technology Inc·April 24, 2013
Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.
FDA Recall
Terminated
·The Anspach Effort, Inc.·Product code MOQ·November 25, 2015
Synthes Matrix Mandible Short Cut Plate Cutter Synthes Matrix Mandible Short Cut Plate Cutter is intended for oral, maxillofacial surgery.
FDA Recall
Terminated
·Synthes, Inc.·Product code HTZ·April 22, 2014
DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various orthopedic procedures
FDA Recall
Terminated
·DePuy Orthopaedics, Inc.·Product code LXH·January 6, 2017
DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The gloves are designed to resist sticks and cuts and are not cut or puncture proof. These gloves are not required by any surgical technique.
FDA Recall
Terminated
·DePuy Orthopaedics, Inc.·Product code FYE·May 8, 2013
PIPELINE LS ACCESS SYSTEM, Holding Clip The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor.
FDA Recall
Terminated
·DePuy Spine, Inc.·Product code GCC·July 31, 2013
PIPELINE LS ACCESS SYSTEM, 2nd Dilator, 10 mm, Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor.
FDA Recall
Terminated
·DePuy Spine, Inc.·Product code GCC·July 31, 2013
PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor.
FDA Recall
Terminated
·DePuy Spine, Inc.·Product code GCC·July 31, 2013
PIPELINE LS ACCESS SYSTEM, 3rd Dilator, 14 mm Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor.
FDA Recall
Terminated
·DePuy Spine, Inc.·Product code GCC·July 31, 2013
PIPELINE LS ACCESS SYSTEM, 4th Dilator, 18 mm, Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling proper placement of the Pipeline LS Retractor.
FDA Recall
Terminated
·DePuy Spine, Inc.·Product code GCC·July 31, 2013
Songer Spinal Cable System, Single Cable, Crimp, Bar, Stainless Steel, Sterile. The DePuy Spine Cable System can be utilized anywhere monofilament wire has been previously found to be indicated.
FDA Recall
Terminated
·RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)·Product code JDQ·May 29, 2015
Light Adaptor for Small Battery Drive and Small Battery Drive II.
FDA Recall
Terminated
·The Anspach Effort, Inc.·Product code HWE·June 24, 2016
The GLOBAL UNITE Platform Shoulder System is intended for cemented or uncemented total shoulder or hemi-shoulder replacement procedures, Product labeling: LEO-1100-30-000 REV D.pdf.pdf, LEO-1100-40-000 REV D.pdf.pdf, LEO-110030100_REV D.pdf.pdf, LEO-110030110_REV D.pdf.pdf, LEO-110030120_REV D.pdf.pdf
FDA Recall
Terminated
·DePuy Orthopaedics, Inc.·Product code KWS·November 28, 2017
Synthes 3.0 MM TI Cannulated Screw Instrument and Implant Set
FDA Recall
Terminated
·Synthes, Inc.·Product code HWC·June 30, 2014
The Synthes Mandible External Fixator; all lots of part nos.: 04.305.003 04.305.004 04.305.005 04.305.010 04.305.011 04.305.012 03.305.006 04.305.100 04.305.101 04.305.102 04.305.103 04.305.128 04.305.130 04.305.134 04.305.138 04.305.140 04.305.142 03.305.105 03.305.500 03.305.500S Intended to stabilize and provide treatment for fractures of the maxillofacial area, including severe open mandibular fractures, highly comminuted closed fractures, nonunions and delayed unions (especially associated with infection), fractures associated with infections, tumor resections, facial deformity corrections, gunshot wounds, pan facial fractures, burn maintenance, and bone grafting defects.
FDA Recall
Terminated
·Synthes, Inc.·Product code MQN·October 17, 2014
2.0 Mandible Locking Plate (MLP) Bender / Cutter (part number 329.143) Intended to be used for bending and/or cutting Mandible Locking Plates.
FDA Recall
Terminated
·Synthes, Inc.·Product code HXW·December 15, 2014
DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level / 57 mm part 04.613.257 lot 3693878 TI Vectra" Plate 4 Level / 64 mm part 04.613.364 lot 8143905
FDA Recall
Terminated
·Synthes, Inc.·Product code KWQ·September 2, 2014
2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE, Part Number 04.210.116TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
FDA Recall
Terminated
·Synthes, Inc.·Product code HRS·December 16, 2019
MatrixNEURO Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial skeleton in procedures such as craniotomies, reconstructive procedures, fracture repair, osteotomies, and selective orthognathic surgery of the maxilla and chin.
FDA Recall
Terminated
·Synthes, Inc.·Product code JEY·June 18, 2020