Events

Rappel de Device Recall Zimmer

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 Manufacturing B.V..

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
    72900
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1151-2016
  • Date de mise en oeuvre de l'événement
    2016-01-11
  • Date de publication de l'événement
    2016-03-12
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2017-04-13
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=143878
  • 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
    As a result of the insufficient sealer calibration data for product packaged in firm's building ii between august 2010 and april 2013. the affected products are sterile.
  • Action
    Zimmer Biomet sent an Urgent Medical Device Recall Letter, dated January 11, 2016, to Distributors, Sales Representatives, Operation Managers, and Risk Managers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to 1.Review the notification and ensure that relevant personnel are aware of the contents. 2. Assist your Zimmer Biomet sales representative with the quarantine of any affected product. 3. Your Zimmer Biomet sales representative will remove the recalled product from your facility. 4. Complete and return the attached Certificate of Acknowledgment form to corporatequality.postmarket@zimmerbiomet.com. 5. If after reviewing this notification you have further questions or concerns please call Customer Service at 1-800-348-2759, or contact your Zimmer Biomet Sales Representative.

Device

Device Recall Zimmer
  • Modèle / numéro de série
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    US Nationwide Distribution
  • Description du dispositif
    Product 53 consists of all product under: product code: JWH and same usage: || Item no: || 597002501 NEXGEN PRECOAT PEG TIB PL || 597002502 NEXGEN PRECOAT PEG TIB PL || 597003501 NEXGEN PRECOAT PEG TIB PL || 597003502 NEXGEN PRECOAT PEG TIB PL || 597004501 NEXGEN PRECOAT PEG TIB PL || 597004502 NEXGEN PRECOAT PEG TIB PL || 597005501 NEXGEN PRECOAT PEG TIB PL || 597005502 NEXGEN PRECOAT PEG TIB PL || 597005503 NEXGEN PRECOAT PEG TIB PL || 597005504 NEXGEN PRECOAT PEG TIB PL || 598002701 NEXGEN PRECOAT STEMMED TI || 598002702 NEXGEN PRECOAT STEMMED TI || 598003701 NEXGEN PRECOAT STEMMED TI || 598003702 NEXGEN PRECOAT STEMMED TI || 598004701 NEXGEN PRECOAT STEMMED TI || 598004702 NEXGEN PRECOAT STEMMED TI || 598005701 NEXGEN PRECOAT STEMMED TI || 598005702 NEXGEN PRECOAT STEMMED TI || 598005703 NEXGEN PRECOAT STEMMED TI || 598005704 NEXGEN PRECOAT STEMMED TI || 598801510 NEXGEN SHARP FLUTED STEM || 598801511 NEXGEN SHARP FLUTED STEM || 598801512 NEXGEN SHARP FLUTED STEM || 598801513 NEXGEN SHARP FLUTED STEM || 598801514 NEXGEN SHARP FLUTED STEM || 598801515 NEXGEN SHARP FLUTED STEM || 598801516 NEXGEN SHARP FLUTED STEM || 598801517 NEXGEN SHARP FLUTED STEM || 598801518 NEXGEN SHARP FLUTED STEM || 598801519 NEXGEN SHARP FLUTED STEM || 598801520 NEXGEN SHARP FLUTED STEM || 598801010 NEXGEN STRAIGHT STEM EXT || 598801011 NEXGEN STRAIGHT STEM EXT || 598801012 NEXGEN STRAIGHT STEM EXT || 598801013 NEXGEN STRAIGHT STEM EXT || 598801014 NEXGEN STRAIGHT STEM EXT || 598801015 NEXGEN STRAIGHT STEM EXT || 598801016 NEXGEN STRAIGHT STEM EXT || 598801017 NEXGEN STRAIGHT STEM EXT || 598801018 NEXGEN STRAIGHT STEM EXT || 598801020 NEXGEN STRAIGHT STEM EXT || 598801022 NEXGEN STRAIGHT STEM EXT || 598801024 NEXGEN STRAIGHT STEM EXT || 598801112 NEXGEN STRAIGHT STEM EXT || 598801113 NEXGEN STRAIGHT STEM EXT || 598801114 NEXGEN STRAIGHT STEM EXT || 598801115 NEXGEN STRAIGHT STEM EXT || 598801116 NEXGEN STRAIGHT STEM EXT || 598801117 NEXGEN STRAIGHT STEM EXT || 598801118 NEXGEN STRAIGHT STEM EXT || 598801212 NEXGEN STRAIGHT STEM EXT || 598801215 NEXGEN STRAIGHT STEM EXT || for use in total knee arthroplasty
  • Manufacturer
    Zimmer Manufacturing B.V.

Manufacturer

Zimmer Manufacturing B.V.
  • Adresse du fabricant
    Zimmer Manufacturing B.V., Turpeaux Industrial Park Rd 1 km 123.4, Mercedita PR 00715
  • 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