{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Memphis",
      "address_1": "1800 Pyramid Pl",
      "reason_for_recall": "The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.",
      "address_2": "",
      "product_quantity": "3",
      "code_info": "P239150",
      "center_classification_date": "20160823",
      "distribution_pattern": "AR, MN,MA",
      "state": "TN",
      "product_description": "RESPONSIVE, KNEE:  FEMORAL  total knee replacement COMPONENT CR/CS, SIZE 4R,  REF 90-SRK-311400, QTY:  1, STERILE R,",
      "report_date": "20160831",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "recall_number": "Z-2632-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74850",
      "termination_date": "20161122",
      "more_code_info": "",
      "recall_initiation_date": "20160718",
      "postal_code": "38132-1703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}