BEUDAMED
    346 results · 17ms · 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 ×

    100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to ethylene oxide sterilization. Tube maintains sterility of the enclosed medical devices until opened.

    FDA Recall
    Terminated ·Steris Corporation·Product code LRT·August 2, 2012

    GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF) FEMORAL COMPONENT NONPOROUS N-K FLX GSF NP FEM SZ 0 RT N-K FLX GSF NP FEM SZ 4 LT N-K FLX GSF NP FEM SZ 4 RT Components with CSTi porous coating are indicated for uncemented or cemented use in skeletally mature individuals with intact medial and lateral collateral ligaments undergoing primary surgery for rehabilitating knees damaged as a result of Noninflammatory Degenerative Joint Disease (NIDJD) or Inflammatory Joint Disease (IJD).

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code JWH·November 29, 2017

    GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM FEMORAL COMPONENT N-K FLX GSM POR FEM SZ 2 RT N-K FLX GSM POR FEM SZ 3 LT N-K FLX GSM POR FEM SZ 4 LT N-K FLX GSM POR FEM SZ 4 RT N-K FLX GSM POR FEM SZ 5 LT N-K FLX GSM POR FEM SZ 5 RT Components with CSTi porous coating are indicated for uncemented or cemented use in skeletally mature individuals with intact medial and lateral collateral ligaments undergoing primary surgery for rehabilitating knees damaged as a result of Noninflammatory Degenerative Joint Disease (NIDJD) or Inflammatory Joint Disease (IJD).

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code MBH·November 29, 2017

    Natural-Knee II Constrained Knee System NKII CCK TIB INS SZ00/0-L NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ3-5 -R NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ1/2-RT NKII CCK TIB INS SZ3-5 -R NKII CCK TIB INS SZ00/0-L NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ3-5 -R NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ3-5 -R NKII CCK TIB INS SZ00/0-L NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ1/2-RT NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ1/2-RT NKII CCK TIB INS SZ00/0-L NKII CCK TIB INS SZ00/0-R

    FDA Recall
    Terminated ·Zimmer, Inc.·Product code JWH·February 25, 2014

    OPTI SARS-CoV-2 RT-PCR Test, REF Numbers: a) 99-57003 b) 99-57004

    FDA Recall
    Open, Classified ·OPTI Medical Systems, Inc·Product code QJR·June 25, 2021

    Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor system. The ANX 3.0 system is comprised of these components. 1. Patient Physiological Monitor, 2. Laptop Computer, 3. Stand w/wheels, 4. Patient cables, 5. Software components (Respiratory and Cardiac Spectral Frequency Signal Processor). The different monitor components that can be used in the system are one of the following per system are as follows: Patient Physiological Monitors used: CJPS Vital Pro, Zoe Medical Nightingale Monitoring system, Ivy Biomedical model 405P, Software components: Ansar ANS C 3000. The device is also referred to as the ANS-C3000.

    FDA Recall
    Terminated ·Ansar Group, Inc. Dba Ansar Medical Technologies, Inc·Product code DRT·July 1, 2014

    Panorama Patient Monitoring Network. Cardiac Arrhythmia Monitor.

    FDA Recall
    Terminated ·Datascope Corp·Product code DRT·June 16, 2005

    Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd

    FDA Recall
    Open, Classified ·Navajo Manufacturing Company·Product code IRT·February 18, 2026

    Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat garment and wraps

    FDA Recall
    Terminated ·2k Innovations Inc.·Product code IRT·April 15, 2016

    Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat garment and wraps

    FDA Recall
    Terminated ·2k Innovations Inc.·Product code IRT·April 15, 2016

    Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment and wraps

    FDA Recall
    Terminated ·2k Innovations Inc.·Product code IRT·April 15, 2016

    HoMedics Thera P Standard size Moist/Dry Heating Pad with Auto Shut-off, Model No. HP-200 (UPC 031262007926).

    FDA Recall
    Terminated ·HoMedics, Inc.·Product code IRT·February 9, 2007

    Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002

    FDA Recall
    Open, Classified ·Whele LLC DBA Perch·Product code IRT·October 24, 2022

    Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps

    FDA Recall
    Terminated ·2k Innovations Inc.·Product code IRT·April 15, 2016

    Vios Monitoring System Bedside Monitor Model BSM2050

    FDA Recall
    Open, Classified ·Murata Vios, Inc.·Product code DRT·August 9, 2024

    Panorama Patient Monitoring Network, Cardiac Arrhythmia Monitor.

    FDA Recall
    Terminated ·Datascope Corp·Product code DRT·August 19, 2005

    muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate

    FDA Recall
    Completed ·Murata Vios, Inc.·Product code DRT·June 21, 2021

    Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00

    FDA Recall
    Open, Classified ·Murata Vios, Inc.·Product code DRT·June 6, 2023

    HoMedics Thera P King size Moist/Dry Heating Pad; Model No. HP-300 (UPC 031262003645).

    FDA Recall
    Terminated ·HoMedics, Inc.·Product code IRT·February 9, 2007

    HoMedics Thera P Standard size Dry Heating Pad; Model No. HP-100 (UPC 031262003621).

    FDA Recall
    Terminated ·HoMedics, Inc.·Product code IRT·February 9, 2007