BEUDAMED
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    WALL MEDICAL, INC.

    FDA registration
    WALL MEDICAL, INC.·2 products·🇺🇸 United States

    ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China

    FDA Enforcement
    Class II ·Terminated·Global Healthcare Inc·February 10, 2016

    ET-20 Anesthesia Extension Tubes, 2.5 ml approximately, Sterile and Disposable, Wall Medical Inc., Made in China

    FDA Recall
    Terminated ·Global Healthcare Inc·Product code FPA·January 6, 2016

    INTRODUCER KIT, GASTROSTOMY FEEDING TUBE, 18FR DILATOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KGC·September 18, 2023

    UNKNOWN, DH EF PERC PLACEMENT PRODUCTS

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KGC·October 1, 2022

    CORFLO NG/NI FEED TUBE WITH STYLET, ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·April 11, 2026

    POWER SUPPLY

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code MRZ·January 31, 2016

    UNK

    FDA Adverse Event
    Malfunction ·DRAEGER MEDICAL SYSTEMS, INC.·Product code DRG·August 14, 2007

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 6, 2026

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 26, 2026

    CORFLO NASOGASTRIC/NASOINTESTINAL FEEDING TUBE WITH STYLET WITH ENFIT CONNECTOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 12, 2026

    UNKNOWN CORPAK NASOGASTRIC TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·October 30, 2025

    Hospira LifeShield Latex-Free 100 mL Burette Set, Convertible Pin, 77 inch with 2 Prepierced Injection Sites and Option-Lok Microdrip Soluset with Calibrated Burette and Precision Drip Chamber; an Rx sterile medical device used to administer fluids; 20 individually wrapped sets per case; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 USA; list 12722-65. Intended use: for the administration of fluids.

    FDA Enforcement
    Class II ·Terminated·Hospira Inc.·August 1, 2012

    MIC GASTROSTOMY FEEDING TUBE WITH ENFIT CONNECTOR

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC·Product code KNT·September 12, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·June 7, 2023

    INTRODUCER KIT FOR GASTROSTOMY FEEDING TUBE, 24FR DILATOR

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KGC·August 15, 2025

    MIC SAFETY PEG KIT WITH ENFIT® CONNECTORS-20 FR-PULL

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·April 10, 2026

    FREESTYLE COMFORT

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code CAW·February 23, 2022

    UNKNOWN NASOGASTRIC TUBES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 6, 2026

    POWER SUPPLY (FIXED HEADS )ASM

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code MRZ·May 23, 2016