BEUDAMED
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    JariTrak Table Clamp, 1 inch diameter, vertical post, Catalog Number 206-160. The JariTrak Table Clamp with vertical post (206-160) is part of the Table Mounted Hardware that is used with the JariTrak™ Retractor System. The JariTrak™ self-retaining retractor system consists of the Table Clamp with Vertical Post, Flexible or Horizontal Bar with Universal Joint, Oval or Segment Rings, Tilting Blade Clamps and various blades. The product is supplied non-sterile and may be packaged individually or as part of the JariTrak™ retractor set.

    FDA Recall
    Terminated ·J. Jamner Surgical Instruments, Inc.·Product code KDC·November 14, 2006

    AOA Mini RPE Screw Assembly , a component of Herbst, MARA and Fixed Metal devices. Product Usage: AOA Mini RPE Screw Assembly is a component of Herbst, MARA and Fixed Metal devices; removable functional appliances that are to modify the growth of the jaws in a prescribed growth pattern, however, this category is generally attached to the patients upper and lower molars or bicuspids by means of temporary stainless steel crowns or orthodontic bands. Retainer, Screw Expansion, Orthodontic.

    FDA Recall
    Terminated ·Sybron Dental Specialties·Product code DYJ·June 6, 2013

    Brius Patient Specific Brackets (components in a set of custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL

    FDA Recall
    Terminated ·Brius Technologies Inc.·Product code DYJ·February 7, 2022

    Generation 4 electronic liquid gauges used on the Caire Liberator, Stroller, Sprint, and Hi-Flow Portable oxygen unit.

    FDA Recall
    Terminated ·Caire, Inc.·Product code BYJ·October 23, 2007

    Customized Brius Appliances (custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL

    FDA Recall
    Terminated ·Brius Technologies Inc.·Product code DYJ·February 7, 2022

    CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit

    FDA Recall
    Terminated ·Caire, Inc.·Product code BYJ·October 10, 2022

    CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit

    FDA Recall
    Terminated ·Caire, Inc.·Product code BYJ·October 10, 2022

    AdvanSync is an orthodontic device intended for the orthodontic treatment of Class II malocclusions. The AdvanSync part numbers and lot numbers affected by this recall are as follows: Part Number: 600-4000 (Kits-include 10 Right 600-4000 and 10 Left Assemblies). Lot Numbers: 070990588, 070976869, 060971515, 060971514, 04094278D Part Number: 600-4040 (5-Pack, Left Assembly). Lot Numbers: 080901333, 080902356, 070981416, 060971299, 060976084 Part Number: 600-4041 (5-Pack, Right Assembly). Lot Numbers: 080902357, 080901335, 070981417, 060971304, 060976079

    FDA Recall
    Terminated ·Ormco Corporation·Product code DYJ·October 2, 2009

    CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit

    FDA Recall
    Terminated ·Caire, Inc.·Product code BYJ·October 10, 2022

    AOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesial Jet, and Uprighter Jet. Removable functional orthodontic appliances that are to modify the growth of the jaws in a prescribed growth pattern.

    FDA Recall
    Terminated ·Allesee Orthodontic Appliances·Product code DYJ·February 24, 2014

    Precision Medical- Easy Mate Portable Liquid Oxygen System (container), PM22010 Series, Model number 2201, Precision Medical, Inc., Northampton, PA 18067

    FDA Recall
    Terminated ·Precision Medical, Inc.·Product code BYJ·October 4, 2006

    Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL

    FDA Recall
    Terminated ·Brius Technologies Inc.·Product code DYJ·February 7, 2022

    CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit

    FDA Recall
    Terminated ·Caire, Inc.·Product code BYJ·October 10, 2022

    1.5 mm Inion CPS, Burrhole plate, REF PLT-1011, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010

    2.0 mm Inion CPS, 4 hole plate, REF PLT-1013, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010

    1.5 mm Inion CPS, 20 hole plate, REF PLT-1007, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010

    2.0 mm Inion CPS, 6 hole plate, REF PLT-1038, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010

    2.5 mm Inion CPS, 8 hole plate, REF PLT-1027, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010

    1.5 mm Inion CPS, 6 hole plate, REF PLT-1006, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010

    2.5 mm Inion CPS, 4 hole plate, REF PLT-1023, sterile, Manufacturer, INION Oy, Finland.

    FDA Recall
    Terminated ·Stryker Craniomaxillofacial Division·Product code JEY·April 14, 2010