{
  "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": "Mercedita",
      "address_1": "Turpeaux Industrial Park Rd 1 km 123.4",
      "reason_for_recall": "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.",
      "address_2": "",
      "product_quantity": "17",
      "code_info": "lot no.:  62065298  62221052  62221052N  62093457  62185967  62268539  62334044  62268539N  61555436  62162471  62221049  62268540  62285362  62268540N  62285362N",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 39 consists of all product under  product code: JDI  and same usage:  Item no:\t  32902605800\tION IMPLANTED FEM 22MM LO  32902604900\tION IMPLANTED FEM 26MM ME  32902603900\tION IMPLANTED FEM 26MM SH    For use in total or hemi hip arthroplasty",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "recall_number": "Z-1137-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72900",
      "termination_date": "20170413",
      "more_code_info": "",
      "recall_initiation_date": "20160111",
      "postal_code": "00715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}