BEUDAMED
    27 results · 14ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall ×

    Package Insert which accompanies the Hematocrit and Metabolite QUALICHECK LEVEL 2 Quality Control of Hematocrits and Metabolites, used with the ABL 77/70/555 Blood Gas & Electrolyte Analyzers. The QC reagents are packaged in a box of 30 glass vials of (1.5 ml) per box. The package insert is packed one per box.

    FDA Recall
    Terminated ·Radiometer America Inc·Product code GKF·May 24, 2005

    16 G / 5F Dual Lumen L-Cath catheter only.

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    16 G / 5F Dual Lumen L-Cath Basic Kit with Introsyte

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    16 G / 5F Dual Lumen L-Cath complete kit with U-Wing

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    16 G / 5F Dual Lumen L-Cath Basic Kit with U-Wing

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    16 G / 5F Dual Lumen L-Cath Basic Kit with Insyte Autoguard

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte Autoguard

    FDA Recall
    Terminated ·Becton Dickinson Medical Systems·Product code LJS·March 25, 2005

    CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.

    FDA Recall
    Terminated ·Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·December 19, 2019

    Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series. The firm name on the label for the HemoPoint H2 shows Manufactured by EKF-diagnostic GmbH, Germany.

    FDA Recall
    Terminated ·Product code GKR·February 8, 2018

    Matrix MAX3 Actuator, Catalog Number: MAX30 A300545A2510V000, SKF USA, Inc. Norristown, PA 19403

    FDA Recall
    Terminated ·Skf USA Inc·July 24, 2007

    Matrix MAX3 Actuator, Catalog Number: MAX30 A300515A254L000, SKF USA, Inc. Norristown, PA 19403

    FDA Recall
    Terminated ·Skf USA Inc·July 24, 2007

    Matrix MAX3 Actuator, Catalog Number : MAX30 A300545A252L0V000, SKF USA, Inc. Norristown, PA 19403

    FDA Recall
    Terminated ·Skf USA Inc·July 24, 2007

    Injection Needle, REF: 25207

    FDA Recall
    Open, Classified ·Karl Storz Endoscopy·Product code GCF·October 24, 2023

    ECONO STERILE medical procedure kits labeled as: ECONO STERILE CEMENT SPATULA #24 STRL CS/25, Model Number 96-2245M, mixing utensil, dental

    FDA Recall
    Open, Classified ·Sklar Instruments·Product code GAF·December 3, 2024

    CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.

    FDA Recall
    Terminated ·Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·December 19, 2019

    ClubMax Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Logolas Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Burstberry Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019

    Atom Laser Projection Series

    FDA Recall
    Open, Classified ·Gk Photonics Inc·Product code REA·July 10, 2019