{
  "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": "0",
      "code_info": "lot no.:  62185968  62273370  62339644  62162469  62279774  62279774N  62221051  62279775  62279775N",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 28 consists of all product under product code: JDI and same usage:  Item no:\t  32902605000\tFEMORAL HD 28MM MEDIUM  32902604000\tFEMORAL HD 28MM SHORT  32902604035\tFEMORAL HD 28MM SHT+ 3.5M    For use in total or hemi hip arthroplasty",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "recall_number": "Z-1126-2016",
      "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"
    }
  ]
}