{
  "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": "6055 Primacy Pkwy Ste 140",
      "reason_for_recall": "Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm.",
      "address_2": "",
      "product_quantity": "20 units",
      "code_info": "Lot Number 101868",
      "center_classification_date": "20170320",
      "distribution_pattern": "Al, FL, IN, Il, NE, TX, NM, CO, AZ",
      "state": "TN",
      "product_description": "MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Crossroads Extremity Systems Llc",
      "recall_number": "Z-1487-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "76687",
      "termination_date": "20170427",
      "more_code_info": "",
      "recall_initiation_date": "20170216",
      "postal_code": "38119-5702",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}