BEUDAMED
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    Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee Femoral Component is intended for use with Signal Medical Corp. Total Knee System for cemented use INA Total Knee Replacement. The femoral component is made of cobalt chromium alloy (ASTM F75).

    FDA Enforcement
    Class II ·Terminated·Signal Medical Corporation·October 29, 2014

    CATH GUIDE 6F MB2 110CM Z2 CATHETER Z26MB2A Z2 6F 110CM MB2 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. Product Code: Z26MB2A

    FDA Recall
    Terminated ·Medtronic, Inc.·Product code DQY·April 5, 2006

    NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272521.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 10, 2006

    NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272519.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 10, 2006

    NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272520.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 10, 2006

    NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272518.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 10, 2006

    NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272522.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code JWH·October 10, 2006

    3M" Steri-Vac" Gas Sterilizer/Aerators, Model #'s 4XL,5XL, 8XL The 3M" Steri-Vac" Gas Sterilizer/Aerator is a compact unit designed to sterilize heat- and/or moisture-sensitive devices. This gas sterilizer/aerator is intended for INDOOR USE ONLY.

    FDA Recall
    Terminated ·3M Company Health Care Business 3M Center·Product code FLF·March 17, 2014

    BOLD/INI-CLIP 2.2mm Drill Bit with AO Attachment.

    FDA Recall
    Terminated ·Integra LifeSciences Corp.·Product code HTW·November 10, 2006

    Jostra Heater Cooler Unit HCU30, system version 1.02-Low voltage machine

    FDA Recall
    Terminated ·MAQUET Inc.·Product code DWC·November 10, 2006

    AXIOM Artis X-ray systems running software versions VB11K and VB22G

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code IZI·March 10, 2006

    Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging Communication Device Model IV - product code 5000230 Model ID, product code 5000330 Konica Minolta Medical & Graphic, Inc. No. 26-2, Nishishinjuku 1-chrome, Shinjuku-ku, Tokoyo 163-0512, Japan

    FDA Recall
    Terminated ·Konica Minolta Medical Imaging USA, Inc.·Product code LMD·October 6, 2006

    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

    Storz Documentation Cart with Articulating Arm, Model Number 9601F

    FDA Recall
    Terminated ·Karl Storz Endoscopy America Inc 600 Corporate Pointe·Product code KOG·March 10, 2006

    Powder Free Latex , Non-sterile Medical Exam Gloves Cat #s: 22401 22402 22403 and 22404

    FDA Recall
    Terminated ·Gulf South Medical Supply Inc·Product code LYY·April 10, 2006

    GE Healthcare-Datex-Ohmeda Aisys Anesthesia Delivery System with Aladin 2 cassettes, GE Healthcare, Madison, WI; Datex-Ohmeda, inc., a General Electric company

    FDA Recall
    Terminated ·Datex Ohmeda, Inc·Product code BSZ·August 10, 2006

    Blood Gas and Co-Ox Electrolyte & Metabolyte Analyzer, ABL-800 series.

    FDA Recall
    Terminated ·Radiometer America Inc·Product code CHL·June 17, 2005

    Blood Gas and Co-Ox Electrolyte & Metabolyte Analyzer, ABL-700 series.

    FDA Recall
    Terminated ·Radiometer America Inc·Product code CHL·June 17, 2005

    Access Immunoassay system CEA, in vitro diagnostic, Part No. 33200

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code DHX·April 12, 2006

    Enpath Lead Adapters, pacemaker lead adapter. Affects: 5 mm Bipolar, Model 501205; 6 mm Unipolar, Model 501204; 3.2 mm Low-Profile Bipolar Models 501206 and 501214. All labeled Sterile, EO, mail: Enpath Medical, Inc. Lead Technologies Division, Minneapolis, MN 55439 USA.

    FDA Recall
    Terminated ·Enpath Medical, Inc·Product code DTB·July 18, 2006