BEUDAMED
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    Adapter for ACMI Hysteroscope Catalog Number: 55035

    FDA Recall
    Terminated ·Boston Scientific Marlbourgh·Product code MNB·July 28, 2005

    Guardian Distal Femur Axial Pin

    FDA Recall
    Terminated ·Wright Medical Technology Inc·Product code JDI·January 3, 2006

    LifeScan OneTouch Ultra Primary Care Physician Demo Kits, Blood Glucose Meter

    FDA Recall
    Terminated ·Lifescan Inc·Product code NBW·October 10, 2005

    Depuy brand LCS Complete metal backed patella, cemented, LRG; REF 1294-09-760.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, porocoat, LRG+; REF 1294-09-670.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, cemented, STD; REF 1294-09-740.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, cemented, STD+; REF 1294-09-750.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, porocoat, STD+; REF 1294-09-650.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, porocoat, LRG; REF 1294-09-660.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, cemented, LRG+; REF 1294-09-770.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Depuy brand LCS Complete metal backed patella, porocoat, STD; REF 1294-09-640.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005

    Panorama Patient Monitoring Network. Cardiac Arrhythmia Monitor.

    FDA Recall
    Terminated ·Datascope Corp·Product code DRT·June 16, 2005

    Tri-Plex Adapter, single unit (MD-04000 )or box of 25 (MD-04001) or case of 100 (MD-04002). Sterile. Single Use.

    FDA Recall
    Terminated ·Medical Device Group Inc.·Product code MOD·June 8, 2005

    Mysis Laboratory version 6.1

    FDA Recall
    Terminated ·Misys Healthcare Systems·Product code JQP·May 10, 2005

    Renegade Hi-Flo Microcatheter Kits, Catalog/Order # 18-299, UPN M001182990

    FDA Recall
    Terminated ·Boston Scientific Corporation One Boston·Product code KRA·August 10, 2005

    MicroScan Rapid Pos Inoculum Broth, Catalog #: B1015-14; Manufactured and distributed by: Dade Behring Inc. 2040 Enterprise Blvd. West Sacramento, CA 95691

    FDA Recall
    Terminated ·Dade Behring·Product code LON·February 7, 2005

    STA Liatest Free Protein S, cat. 00516. These kits are intended for use with analyzers of the STA brand name for the quantitative determination of free protein S in plasma by the immuno-turbidimetric method.

    FDA Recall
    Terminated ·Diagnostica Stago, Inc.·Product code GGP·October 26, 2005

    TOSOH ST AIA- PACK TT3, Lot FX17440, catalog #025282. This reagent is used for the quantitative measurement of Total Triiodothyronine Human Serum. Each box of product contains 5 trays of 20 test cups per tray. Each tray is packaged in a foil pack. Both the box and foil packs have product labels.

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code CDP·January 26, 2006

    Discovery ST PET/CT imaging system with gantry model number 5105797. Catalog Identifiers: S9114LA/LB/MA/MN, S9118LA/LB/MA/MN, S9116LA/MA. The system combines the high performance Lightspeed Plus CT with high performance PET that is optimized for routine 2D and 3D oncology, cardiology and neurology clinical studies.

    FDA Recall
    Terminated ·General Electric Med Systems LLC·Product code KPS·January 26, 2006

    OTC Pregnancy Test labeled ''CHOICE Pregnancy Test Kit'' (PA-410A), midstream, no cups or droppers. Label reads: ''One Step, Easy to Use, Positive result as early as 1 minute, Over 99% accurate.'' Each box contains one home test kit. Responsible firm on label: Distributed by ICC, Amherst, NY 14228.

    FDA Recall
    Terminated ·International Chemical Inc.·Product code LCX·October 7, 2004