{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "M/L Taper Hip Prosthesis and M/L Taper Hip Prosthesis with Kinectiv Technology manufactured prior to October 2015 are being recalled due to the potential for black residue to be observed within the polyethylene bag containing the implant. The black residue is a combination of the titanium plasma spray used to create the porous surface of the implant and polyethylene bag containing the implant. The recalling firm states the residue is biocompatible. Risks include delay of surgery while locating a replacement device, and surgical intervention due to wear caused by debris.",
      "address_2": "",
      "product_quantity": "1024",
      "code_info": "61288759  61542760  61710043  61729725  61735130  61768446  61805951  61843648  61874222  61950885  61957017  61967640  61967642  61985977  62010557  62014550  62059104  62124960  62134980  62153554  62163677  62191383  62225911  62270944  62273474  62275220  62275874  62316364  62329143  62356225  62418056  62420829  62420831  62420832  62432973  62472159  62503173  62521423  62521424  62521425  62521426  62540539  62571382  62578409  62652963  62659314  62659315  62667476  62700958  62721036  62739979  62761717  62776407  62787314  62787315  62794382  62815408  62836783  62836785  62885067  62939020  62939021  62939023  63044942  63051893  63063344  63063345  63063346  63063348  63068961  63068965  63068967  63068969  63076579  63076580  63081284  63081286  63090043  63090044  63094542  63102029  63102030  63108843  63174078  63174079  63174081  77004214  61429027R  62066989R  62335432R  62836786R",
      "center_classification_date": "20180705",
      "distribution_pattern": "Products were distributed solely to Japan.",
      "state": "IN",
      "product_description": "Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 15; 00-7713-015-00",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2369-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "80188",
      "termination_date": "20200528",
      "more_code_info": "",
      "recall_initiation_date": "20180530",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}