BEUDAMED
    55 results · 20ms · 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 × Status: Terminated × Clear all

    VERSYS 6 INCH BEADED FC 1 VERSYS 6 INCH BEADED FC S VERSYS 8 INCH BEADED FC 1 VERSYS 8 INCH BEADED FC 2 prosthesis, hip, semi-constrained, metal/polymer, porous uncemented "" Total hip replacement for the following: severe hip pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders, avascular necrosis of the femoral head, nonunion of previous fractures of the femur; congenital hip dysplasia, protrusio acetabuli, slipped capital femoral epiphysis; disability due to previous fusion; previously failed endoprostheses, and/or total hip components in the affected extremity and acute femoral neck fractures. " Hemi-hip replacement for the following: fracture dislocation of the hip; elderly, debilitated patients when a total hip replacement is contraindicated; irreducible fractures in which adequate fixation cannot be obtained; certain high subcapital fractures and comminuted femoral neck fractures in the aged; nonunion of femoral neck fractures; secondary avascular necrosis of the femoral head; pathological fractures of the femoral neck; and osteoarthritis in which the femoral head is primarily affected."

    FDA Recall
    Terminated ·Zimmer Biomet, Inc.·Product code LPH·January 11, 2016

    EUB-6500/HI VISION 6500 Diagnostic Ultrasound Scanners, DICOM Option EZU-FC5, Software Versions: V01-03, V01-05, V02-04, V03-02, V04-02, V04-03, V04-04, V05-03, V05-05A, V05-07A and V05-30A.

    FDA Recall
    Terminated ·Hitachi Medical Systems America Inc·Product code ITX·May 12, 2008

    The Guardian Connect App CSS7200 iOS - Product Usage: intended for use by patients with a compatible consumer mobile device.

    FDA Recall
    Terminated ·Medtronic Inc.·Product code MDS·July 15, 2020

    ReadyMed Elastomeric Ambulatory Pump, Model Numbers: R050050, R100100, R100200, R250050, R250100, and R250167. Intended for self-administration of anti-microbial and antiviral agents.

    FDA Recall
    Terminated ·Cardinal Health 303 dba Cardinal Health·Product code FRN·December 19, 2008

    Freedom Designs TriPod w/Anti tipper Manual Wheelchair, Models Numbers: TriPod, Tripod LT and TriPod Pediatric LT with Trailing Anti-Tipper-Caster-Axle Link, Freedom Designs Incorporated, Simi Valley, CA 93065

    FDA Recall
    Terminated ·Freedom Designs Inc·Product code IOR·May 14, 2007

    MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.

    FDA Recall
    Terminated ·Medtronic Inc.·Product code OZO·May 8, 2017

    MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.

    FDA Recall
    Terminated ·Medtronic Inc.·Product code OZP·May 8, 2017

    MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.

    FDA Recall
    Terminated ·Medtronic Inc.·Product code OZO·May 8, 2017

    Product's marketing brochure is labeled in part: "Philips Easy Diagnost Eleva Conventional R/F system...PHILIPS". manufactured by Philips Medical Systems Gmbh, Hamburg, Germany.

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code KPR·January 21, 2009

    MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.

    FDA Recall
    Terminated ·Medtronic Inc.·Product code OZP·May 8, 2017

    Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 55, Catalog Number LG-PR0855, Allez Spine, LLC., Irvine, CA

    FDA Recall
    Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

    Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 80, Catalog Number LG-PR0880, Allez Spine, LLC., Irvine, CA

    FDA Recall
    Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

    Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 45, Catalog Number LG-PR0845, Allez Spine, LLC., Irvine, CA

    FDA Recall
    Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

    Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 35, Catalog Number LG-PR0835, Allez Spine, LLC., Irvine, CA

    FDA Recall
    Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

    Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 50, Catalog Number LG-PR0850, Allez Spine, LLC., Irvine, CA

    FDA Recall
    Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

    Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 40, Catalog Number LG-PR0840, Allez Spine, LLC., Irvine, CA

    FDA Recall
    Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

    VACLOCK Syringe, 10ml, REF: VAC110, Sterile EO, Single Use, Merit Medical Systems, Inc., South Jordan, Utah 84095.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code FMF·October 22, 2010

    VACLOCK Syringe, 20ml, REF: VAC120E, Sterile EO, Single Use, Merit Medical Systems, Inc., South Jordan, Utah 84095.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code FMF·October 22, 2010

    Merit MEDALLION Syringe, 10ml, REF: MSSW11-R, Sterile EO, Single Use, Merit Medical Systems, Inc., South Jordan, Utah 84095.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code FMF·October 22, 2010

    Merit MEDALLION Syringe, 10ml, REF: MSSW11-Y, Sterile EO, Single Use, Merit Medical Systems, Inc., South Jordan, Utah 84095.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code FMF·October 22, 2010