10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
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Metha(R) Hip System Cobalt Chrome (CoCr) Metha Modular Neck Adapters used with the Metha Modular Short Hip Stems. Aesculap AG. Intended to replace a hip joint
FDA Recall
Terminated
·Aesculap Inc·Product code LZO·July 19, 2011
Flexible Drill; SJ723R; NON STERILE; B Braun Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
FDA Enforcement
Class II
·Terminated·Aesculap, Inc.·December 30, 2015
Flexible Bone Awl; SJ607R; NON STERILE; B Braun Aesculap; Aesculap AG: These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
FDA Enforcement
Class II
·Terminated·Aesculap, Inc.·December 30, 2015
Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
FDA Enforcement
Class II
·Terminated·Aesculap, Inc.·December 30, 2015
Flexible Drill; SJ723R; NON STERILE; B Braun Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
FDA Recall
Terminated
·Aesculap, Inc.·Product code LRZ·November 10, 2015
Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
FDA Recall
Terminated
·Aesculap, Inc.·Product code LRZ·November 10, 2015
Flexible Bone Awl; SJ607R; NON STERILE; B Braun Aesculap; Aesculap AG: These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
FDA Recall
Terminated
·Aesculap, Inc.·Product code LRZ·November 10, 2015
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
FDA Recall
Terminated
·Aesculap, Inc.·Product code GEI·January 18, 2013
Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is intended to be used for circumcision surgeries
FDA Recall
Terminated
·Aesculap Implant Systems LLC·Product code HFX·October 28, 2016
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
FDA Recall
Terminated
·Aesculap, Inc.·Product code GAD·July 16, 2013