BEUDAMED
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    Pediatric care bed; Product Designation: KayserBett IDA;

    FDA Recall
    Open, Classified ·KAYSERBETTEN GMBH & CO. KG Rieper Str. 12 Bad Fallingbostel Germany·Product code FNL·May 4, 2026

    ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device

    FDA Recall
    Open, Classified ·J & T Health and Wellness LLC·Product code LEJ·March 31, 2023

    Bausch & Lomb * ReNu with MoistureLoc, Multi-purpose soft contact lens solution * Sterile * Manufactured by: Bausch & Lomb, Rochester, NY 14609.

    FDA Recall
    Terminated ·Bausch & Lomb·Product code LPN·April 13, 2006

    NeuViz Dual series computed Tomography Scanner System, X-Ray System The CT scanner is a whole body x-ray computed tomography scanner which features a continuously rotating tube-detector system and functions according to the fan beam principle.

    FDA Recall
    Terminated ·Philips And Neusoft Medical Systems Co., Ltd. Neusoft Park, Hun Nan Industrial Area Shenyang, Liaoning China·Product code JAK·December 17, 2007

    The device is the NeuViz Dual series Computed Tomography (CT) Scanner System. The device is identified as NeuViz Dual, PN: 989605651321. Labeling on the device reads in part: "***Neusoft NeuViz Dual MULTI-SLICE CT SCANNER SYSTEM***MANUFACTURED BY PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD. ADDRESS: NEUSOFT PARK, HUN NAN INDUSTRIAL AREA, SHENYANG 110179, CHINA***". Device is intended to produce cross-section images of head and body by computer reconstruction of x-ray transmission data taken at different angles.

    FDA Recall
    Terminated ·Philips And Neusoft Medical Systems Co., Ltd. Neusoft Park, Hun Nan Industrial Area Shenyang, Liaoning China·Product code JAK·February 10, 2010

    BD Microtainer Tube with Glycolytic Inhibitor, Catalog Number 365992, Non Sterile, 200 (4 x 50), 25 degrees C, Becton Dickinson and Company, Franklin Lakes, NJ

    FDA Recall
    Terminated ·Becton Dickinson & Company·May 17, 2007

    BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel performed on the BD MAX System is an automated in vitro diagnostic test for the direct qualitative detection and differentiation of enteric bacterial pathogens.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code PIC·January 14, 2019

    The product is a battery operated toothbrush. Spinbrush Pro Whitening Ex Soft battery operated toothbrushes UPC 76687800191.

    FDA Recall
    Terminated ·Proctor & Gamble Co·Product code JEQ·February 23, 2005

    The product is a battery operated toothbrush. Spinbrush Pro Ex Soft battery operated toothbrushes UPC 76687800078

    FDA Recall
    Terminated ·Proctor & Gamble Co·Product code JEQ·February 23, 2005

    JOURNEY " UNI TIBIAL INSERT RIGHT MEDIAL/ LEFT LATERAL, A/P 46 MM, M/L 27 MM, REF 71933298, QTY: (1), STERILE EO, SMITH & NEPHEW, INC. MEMPHIS, TN 38116

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code HSX·January 23, 2009

    JOURNEY " UNI TIBIAL INSERT LEFT MEDIAL/ RIGHT LATERAL, A/P 46 MM, M/L 27 MM, REF 71422254, QTY: (1), STERILE EO, SMITH & NEPHEW, INC. MEMPHIS, TN 38116

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code HSX·January 23, 2009

    CLAY ADAMS Dynac III Centrifuge, 120V, Model Number 420104 DYNAC III is a multi-purpose centrifuge, designed for clinical laboratories performing separations in hematology, chemistry, urinalysis, blood banking, microbiology and cytology.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JQC·August 17, 2009

    6 MM X 50 MM X 150 MM HA COATED HALF PIN, 1.6 MM CANNULATED, SST, REF 71070822, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code JDW·April 13, 2012

    6.5 MM CANELLOUS TAP W/ QUICK CONNECT, REF 71173509, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code HWX·April 13, 2012

    6 MM X 45 MM X 150 MM HA COATED HALF PIN SST, REF 71070835, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code JDW·April 13, 2012

    6 MM X 25 MM X 200 MM HA COATED HALF PIN SST, REF 71070803, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

    FDA Recall
    Terminated ·Smith & Nephew Inc·Product code JDW·April 13, 2012

    NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

    FDA Recall
    Terminated ·Codman & Shurtleff, Inc.·Product code DQY·January 11, 2013

    NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

    FDA Recall
    Terminated ·Codman & Shurtleff, Inc.·Product code DQY·January 11, 2013

    NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

    FDA Recall
    Terminated ·Codman & Shurtleff, Inc.·Product code DQY·January 11, 2013

    NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

    FDA Recall
    Terminated ·Codman & Shurtleff, Inc.·Product code DQY·January 11, 2013