Events

Rappel de NEXGEN COMPLETE KNEE SOLUTION MIS TIBIAL COMPONENTS, LOCKING SCREW AND STEM EXTENSIONS

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Zimmer Inc..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    55876
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2413-2010
  • Date de mise en oeuvre de l'événement
    2010-04-26
  • Date de publication de l'événement
    2010-09-13
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2011-03-28
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=92122
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH
  • Cause
    The firm has received complaints of loosening of the implanted device requiring revision surgery. there have been 114 mdrs filed all reported that the device loosened and the patient required additional surgery to replace the device.
  • Action
    The firm, Zimmer, Inc., sent an "URGENT DEVICE CORRECTION" letter dated April 26, 2010, to all customers. The letter described the product, problem and action to be taken by customers. The customers were instructed to destroy or disregard all previous versions of the surgical technique, review the attached revised surgical technique to familiarize yourself with the modifications and warnings, and complete and return the Health Care Professional Dcoumentation Form via fax to Zimmer, Inc. at (574) 372-4265. (Note: Zimmer made a modification to the surgical technique and instructions for use. They added a warning to fully cement and pressurize the anterior and posterior surfaces of the tibial component, and to strongly recommend the use of a drop down stem extension. This change was completed and approved on April 23, 2010.) For questions please contact Zimmer at 1-877-946-2761.

Device

NEXGEN COMPLETE KNEE SOLUTION MIS TIBIAL COMPONENTS, LOCKING SCREW AND STEM EXTENSIONS
  • Modèle / numéro de série
    102316, 103589, 105229, 111084, 111117, 111132, 114008, 7879168, 60218031, 60232196, 60238701, 60251632, 60251633, 60256229, 60258863, 60258864, 60260767, 60264880, 60264881, 60264888, 60267802, 60267803, 60267804, 60269824, 60269825, 60273910, 60273911, 60299534, 60299535, 60302292, 60302293, 60307224, 60307225, 60312265, 60315649, 60317612, 60317613, 60321954, 60326191, 60326192, 60331383, 60331384, 60331385, 60334531, 60334532, 60336060, 60339646, 60339647, 60350415, 60352917, 60355711, 60355712, 60358835, 60362093, 60365656, 60365657, 60372792, 60374325, 60374335, 60380761, 60380762, 60380763, 60384327, 60393079, 60490385, 60492612, 60502854, 60512209, 60518614, 60528088, 60528089, 60548472, 60548473, 60553230, 60555004, 60555005, 60558668, 60562941, 60570906, 60575477, 60578776, 60582743, 60584745, 60584752, 60595807, 60599414, 60608107, 60612405, 60621129, 60625486, 60627679, 60627680, 60631140, 60634795, 60634796, 60644382, 60649157, 60662636, 60667953, 60677462, 60682189, 60692574, 60692582, 60701931, 60706413, 60711161, 60722698, 60748251, 60752977, 60752978, 60756488, 60760515, 60765129, 60770659, 60782870, 60782871, 60790435, 60805429, 60805434, 60809063, 60818766, 60823408, 60836384, 60840795, 60854120, 60854129, 60867944, 60881691, 60881703, 60895103, 60895113, 60895114, 60917513, 60917516, 60929871, 60934277, 60934284, 60942497, 60955231, 60959686, 60968004, 60969502, 60969517, 60983706, 60994899, 61000885, 61006373, 61013840, 61018489, 61034996, 61035006, 61050236, 61057521, 61097038, 61100571, 61105894, 61113640, 61116571, 61121509, 61128973, 61128974, 61138446, 61154236, 61164690, 61164693, 61174186, 61174199, 61187792, 61198692, 61198697, 61204964, 61216065, 61225955, 61231005, 61235903, 61248776, 61253732, 61259042, 61259055, 61259056, 61262899, 61262901, 61262902, 61267821, 61267822, 61267823, 61267838, 61267839, 61267840, 61272596, 61277586, 61277587, 61280554, 61280558, 61280574, 61280575, 61285888, 61289992, 61295482, 61298632, 61298633, 61302105, 61302114, 61307082, 61307083, 61311095, 61311096, 61311112, 61315703, 61315704, 61319847, 61319848, 61324493, 61324504, 61329251, 61329252, 61329253, 61334563, 61334564, 61355741, 61355742, 61360857, 61360858, 61365246, 61365247, 61370255, 61370256, 61376586, 61376596, 61380433, 61380434, 61386647, 61386648, 61395041, 61395042, 61397695, 61399701, 61399702, 61412378, 61412379, 61412380, 61412381, 60732I59 and 61198692R.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide distribution: USA including states of AZ, IL, IN, KY, MO, NE, NM, NY, OH, TX, VA, WA, and WI; and countries of Austria, Belgium, France, Germany, Italy, Netherlands, Spain, Sweden, Switzerland, UK, Ausralia, China, Hong Kong, India, Japan, Korea, Malaysia, Nicaragua, Singapore, Tawain and Thailand.
  • Description du dispositif
    NexGen complete knee solution MIS total knee procedure stemmed tibial component fixed bearing precoat size 6, sterile, REF 00-5950-047-02, Zimmer Inc. Warsaw, IN. || This device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. Collage disorders, and/or avascular necrosis of the femoral condyle. Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy. Moderate valgus, varus, or flexion deformities. The salvage of previously failed surgical attempts or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery. NexGen TM Tibial Trays may be used with or without bone cement (biological fixation). NexGen MIS Tibial Components and MIS Modular Tibial Plates and Keels are intended for cemented use only.
  • Manufacturer
    Zimmer Inc.

Manufacturer

Zimmer Inc.
  • Adresse du fabricant
    Zimmer Inc., 1800 W Center St, Warsaw IN 46580-2304
  • Société-mère du fabricant (2017)
    Zimmer Biomet Holdings
  • Commentaire du fabricant
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    USFDA