{
  "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:  224595  224598  224607  224608  224610  224613  224615  224621  224622  224623  224624  224625  224626  224644  224649  224651  224655  224656  224658  224659  224666, and   224667.",
      "center_classification_date": "20170525",
      "distribution_pattern": "Nationwide distribution only.",
      "state": "PR",
      "product_description": "10-1335M - SpF-XL IIB 2/DM 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-2118-2017",
      "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"
    }
  ]
}