{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Flowood",
      "state": "MS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87661",
      "recalling_firm": "Zavation",
      "address_1": "220 Lakeland Pkwy",
      "address_2": "",
      "postal_code": "39232-9552",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US nationwide distribution.",
      "recall_number": "Z-1741-2021",
      "product_description": "10G DOUBLE CEMENT DELIVERY KIT (8 FILLERS).  For use in Orthopedic / spinal procedures.",
      "product_quantity": "",
      "reason_for_recall": "Products distributed as sterile may not have been adequately sterilized",
      "recall_initiation_date": "20210325",
      "center_classification_date": "20210601",
      "termination_date": "20230320",
      "report_date": "20210609",
      "code_info": "Pending",
      "more_code_info": ""
    }
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}