BEUDAMED
    163 results · 19ms · 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 ×

    Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000

    FDA Recall
    Open, Classified ·Covidien·Product code CCW·September 28, 2023

    Cardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG Electrode Rx Only Single Patient Use Only Manufactured for Cardio Medical Products 385 Franklin Avenue, Suite L Rockaway, New Jersey 07866 www.cardiomedicalproducts.com (800) 227-3633 (973) 586-9624 FAX Defibrillator

    FDA Recall
    Terminated ·Cardio Medical Products·Product code LDD·April 26, 2013

    Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis

    FDA Recall
    Open, Classified ·Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany·Product code LZD·December 6, 2022

    Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.

    FDA Recall
    Terminated ·Covidien LLC·Product code DRO·April 8, 2013

    Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles

    FDA Recall
    Terminated ·Covidien LLC·Product code LRO·September 29, 2016

    Covidien Devon Light Glove packaged in sterile surgical kits Reference: 31140208 Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles

    FDA Recall
    Terminated ·Covidien LLC·Product code LRO·September 29, 2016

    Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550P. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.

    FDA Recall
    Terminated ·Covidien LLC·Product code DRO·April 8, 2013

    Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number S101010

    FDA Recall
    Open, Classified ·Product code GCJ·March 1, 2023

    Mild Chromic Gut Absorbable Sutures, CH GUT 5-0 12 UD SS-14 SS-14 (G-1766-K), CHROMIC GUT 6-0 45CM HE-1 X12 (G-1780K)

    FDA Recall
    Open, Classified ·Product code GAL·March 1, 2023

    Plain Gut Absorbable Sutures, PLAIN GUT 5/0 18 P-13 X12 (SG-5686), PLAIN GUT 4-0 18 UD SC-11 DA (SG828-2)

    FDA Recall
    Open, Classified ·Product code GAL·March 1, 2023

    MEDPOR PLUS SST EZ 22mm Sphere Implant, Howmedica Osteonics Corp, 15 Dart Road, Newnan, GA 30265. MEDPOR PLUS Orbital Implants are intended to restore the volume of an enucleated or eviscerated eye globe.

    FDA Recall
    Terminated ·Howmedica Osteonics Corp dba Stryker Craniomaxillofacial·Product code HPZ·March 20, 2012

    QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System

    FDA Recall
    Terminated ·Stryker Leibinger GmbH & Co. KG Botzinger Strasse 41 Freiburg Germany·Product code GCY·January 3, 2017

    Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove Item Number Description 380789003 SURE SET SINGLE BASIN PACK 400383006 MAJOR BASIN PACK 400383007 MAJOR BASIN PACK 618275004 BASIN PACK Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles

    FDA Recall
    Terminated ·Covidien LLC·Product code LRO·September 29, 2016

    9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silicone, Non-Sterile) 9952 Extended Contoured, Malar Sizer Set (Silicone, Non-Sterile) 85000 Petite Nasal Dorsum Sizer Set (Silicone, Non-Sterile) Accessories to Medpor Implants

    FDA Recall
    Terminated ·Stryker Leibinger GmbH & Co. KG Botzinger Strasse 41 Freiburg Germany·Product code GCY·January 3, 2017

    Delta Cup Beater Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System

    FDA Recall
    Completed ·Limacorporate S.p.A Via Nazionale 52 Frazione Villanova San Daniele del Friuli Italy·Product code LXH·September 8, 2017

    MONOJECT Blood Collection Tubes containing heparin 10x64 Sodium Heparin Item code 8881320256

    FDA Recall
    Terminated ·Product code JKA·November 15, 2010

    MONOJECT Blood Collection Tubes containing heparin 13x100 sodium heparin trace element Item Code 8881307014

    FDA Recall
    Terminated ·Product code JKA·November 15, 2010

    MONOJECT Blood Collection Tubes containing heparin 10x50 Sodium Heparin Item code 8881320157

    FDA Recall
    Terminated ·Product code JKA·November 15, 2010

    Chromic Gut Absorbable Sutures, SURGIGUT* 0 CHR GS-25 90CM X36 (CG-904), SURGIGUT* 1 CHR GS-24 90CM X36 (CG-915), CHROMIC GUT 4-0 75CM V20 (GG-121), CHROMIC GUT 3-0 75CM V20 X36 (GG-122), CHROMIC GUT 2-0 75CM V20 X36 (GG-123), CHROMIC GUT 2-0 75CM V26 (GG-127), CHROMIC GUT 4-0 45CM P12 X36 (SG-5637), CHROMIC GUT 5-0 45CM P-13 X12 (SG-5687G), CHROMIC GUT 5-0 75CM CV23 (UG-202), CHROMIC GUT 4-0 75CM CV23 X36 (UG-203)

    FDA Recall
    Open, Classified ·Product code GAL·March 1, 2023

    AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.

    FDA Recall
    Open, Classified ·SonarMed Inc·Product code OQU·March 21, 2024