BEUDAMED
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    Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; ProSpeed AI; ProSpeed AII; ProSpeed FI; ProSpeed FII; ProSpeed EII; CT HiSpeed Series.

    FDA Recall
    Terminated ·General Electric Med Systems LLC·Product code IXR·October 21, 2004

    Baxter System 1000 Single Patient Hemodialysis Delivery System; Model SYS1000; all series 1000 instruments labeled as System 1000, AltraTouch 1000, Baxter Tina and Baxter Aurora; Baxter Healthcare Corporation, Deerfield, IL 60015 USA or Baxter Healthcare Corporation, McGaw Park, IL 60085 USA

    FDA Recall
    Terminated ·Baxter Healthcare Renal Div·Product code FII·February 20, 2004

    System 1000 family of Hemodialysis Instruments, including the System 1000, Arena, 1550, BM11, BM25 and Meridian; Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A.

    FDA Recall
    Terminated ·Baxter Healthcare Renal Div·Product code FII·December 14, 2004

    Product 34 consists of all product under product code: JWH and same usage: Item no: 522001700 I/B II KNEE DOMED PATELLA 522001800 I/B II KNEE DOMED PATELLA 522001900 I/B II KNEE DOMED PATELLA for use in total knee arthroplasty

    FDA Recall
    Terminated ·Product code JWH·January 11, 2016

    I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGII KNEE SLF-TAP BONE ST

    FDA Recall
    Terminated ·Zimmer, Inc.·Product code JWH·October 11, 2013

    Product 34 consists of all product under product code: JWH and same usage: Item no: 522001700 I/B II KNEE DOMED PATELLA 522001800 I/B II KNEE DOMED PATELLA 522001900 I/B II KNEE DOMED PATELLA for use in total knee arthroplasty

    FDA Enforcement
    Class II ·Terminated·Zimmer Manufacturing B.V.·March 23, 2016

    I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGII KNEE SLF-TAP BONE ST

    FDA Enforcement
    Class II ·Terminated·Zimmer, Inc.·February 26, 2014

    Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED ROD, 1 for use in total knee arthroplasty

    FDA Recall
    Terminated ·Product code JWH·January 11, 2016

    STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles.

    FDA Recall
    Terminated ·Advanced Sterilization Products·Product code FRC·April 22, 2013

    Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED ROD, 1 for use in total knee arthroplasty

    FDA Enforcement
    Class II ·Terminated·Zimmer Manufacturing B.V.·March 23, 2016

    MultiDiagnost MD4

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    LithoDiagnost

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    Diagnost 96/97 DSI

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    UroDiagnost

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    MultiDiagnost MD3

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    EasyDiagnost

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    Easy Diagnost Digital

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    OmniDiagnost

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    Diagnost 76

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009

    ***REF IFNT611***Full OSSEOTITE Tapered Certain Implant 6 x 11.5mm***Sterile by radiation***Rx Only***BIOMET 3i Dental Iberica S.L. WTC Almeda Park, Ed, 1, Planta 1 Pl. de la Pau s/n08940 Cornella de Llobregat (Barcelona) Spain. Lot #2011110798. Intended for surgical placement in the upper or lower jaw to provide a means for prosthetic attachment in single tooth restorations and in partially or fully endentulous spans with multiple single teeth utilizing delayed or immediate loading or with a terminal or intermediary abutment for fixed or removable bridge work and to retain over dentures.

    FDA Enforcement
    Class II ·Terminated·Biomet 3i, LLC·August 15, 2012