BEUDAMED
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    GLOBAL PLASTICS, INC.

    FDA registration
    GLOBAL PLASTICS, INC.·1 product·🇺🇸 United States

    Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch Allyn Inc., 4341 State Street Road, Skaneateles Falls, NY 13153 --- Microlife Corporation 9F, 431, RuiGuang Road, NeiHu, Taipei, 11492, Taiwan, R.O.C. --- Microlife AG Espenstrasse 139 9443 Widnau, Switzerland

    FDA Enforcement
    Class II ·Terminated·Welch Allyn Inc·April 19, 2017

    BACT/ALERT MP BLOOD CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code JTA·August 7, 2008

    WHITESTAR SIGNATURE

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING USA, LLC·Product code HQC·May 11, 2023

    UNK TISSUE EXPANDER

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code LCJ·December 10, 2020

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·December 11, 2020

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·December 9, 2020

    UNK TISSUE EXPANDER

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code LCJ·December 10, 2020

    LIFE01- ORGAN RECOVERY OR PACK

    FDA Adverse Event
    Malfunction ·AVID MEDICAL, INC.·Product code LRO·October 15, 2025

    DERMABOND UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code MPN·June 7, 2024

    UNK - SCREWS: TRAUMA

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·June 8, 2023

    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

    3.5 MM X 191 MM DRILL, REF 71173806, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

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

    3.2 MM IMHS(R) CP SHORT BRAD POINT DRILL, REF 71687001, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

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

    LARGE JOYSTICK THREADED PIN, REF 71173339, 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

    PELVIS PIN, REF 71366302, 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

    2.0 MM X 191 MM DRILL, REF 71173802, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

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

    2.7 MM X 191 MM DRILL, REF 71173804, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

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

    3.2 MM LONG GRADUATED BRAD POINT DRILL, REF 71780105, QTY: (1), STERILE R, Smith & Nephew, Inc., Memphis, TN 38116 Orthopedic surgical device.

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

    ACETABULAR PIN, REF 71366301, 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