{
  "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": [
    {
      "status": "Terminated",
      "city": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75858",
      "recalling_firm": "Amendia, Inc",
      "address_1": "1755 W Oak Pkwy",
      "address_2": "N/A",
      "postal_code": "30062-2260",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution to AL, AZ, AR, CA, CO, FL, GA, IA, KS, KY, LA, MA, MI, MN, MO, NV, NJ, NC, SC, TN, TX, VA, WA, WV, WI and Puerto Rico",
      "recall_number": "Z-0882-2017",
      "product_description": "Dual Stylet Needle, Part Number 812-11R-15  The guide wire is passed through the cannulated handle of the Dual Stylet Needles and pressed into the bone",
      "product_quantity": "1078 units",
      "reason_for_recall": "The rods are packaged in packages with unacceptable seals.  In some cases, the integrity of the seal is compromised by channels or voids.",
      "recall_initiation_date": "20161122",
      "center_classification_date": "20161222",
      "termination_date": "20240201",
      "report_date": "20161228",
      "code_info": "Part Number 812-11R-15  Lot Number 121945, 123231, 124146, 125418, 126822, 127868, 128459, 128464, 130818, 131492, 13496, 132594, 132813, 134514, 134515, 134517, 134909, 135290, 137302"
    }
  ]
}