{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Memphis",
      "address_1": "1800 Pyramid Pl",
      "reason_for_recall": "The Extra Small INFUSE Bone Graft kit from lot M111806AAA, may contain two absorbable collagen sponges (ACS), but should only contain one ACS.",
      "address_2": "",
      "product_quantity": "138 units",
      "code_info": "UDI 00613994239525, Lot Number M111806AAA",
      "center_classification_date": "20181109",
      "distribution_pattern": "US",
      "state": "TN",
      "product_description": "INFUSE Bone Graft X SMALL KIT REF 7510100",
      "report_date": "20181121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "recall_number": "Z-0440-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81171",
      "termination_date": "20200916",
      "more_code_info": "",
      "recall_initiation_date": "20180927",
      "postal_code": "38132-1703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}