{
  "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": "Guaynabo",
      "address_1": "484 Calle E",
      "reason_for_recall": "Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels found during routine process monitoring with the product.",
      "address_2": "",
      "product_quantity": "33 units total",
      "code_info": "Serial Numbers:  410093  410094  410096  410103  410111  410115  410119  410148  410151  410158, and   410171.",
      "center_classification_date": "20170525",
      "distribution_pattern": "Nationwide distribution only.",
      "state": "PR",
      "product_description": "10-1398M - SpF-PLUS Implantable Stimulator.    Indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels.",
      "report_date": "20170531",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "EBI Patient Care, Inc.",
      "recall_number": "Z-2119-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77089",
      "termination_date": "20181017",
      "more_code_info": "",
      "recall_initiation_date": "20170420",
      "postal_code": "00969-3454",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}