{
  "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": "Dania",
      "address_1": "1855 Griffin Rd Ste A310",
      "reason_for_recall": "Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.",
      "address_2": "",
      "product_quantity": "41 devices",
      "code_info": "Lot numbers 20568, 20575, 20581, 20584, 20621, 20623, and 20628, UDI 00816818021430.",
      "center_classification_date": "20181005",
      "distribution_pattern": "Distribution was made CA, FL, IL, IN, MI, NY, and NC.   Foreign distribution was made to Australia.  There was no government/military distribution.",
      "state": "FL",
      "product_description": "OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.",
      "report_date": "20181017",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Orthosensor, Inc.",
      "recall_number": "Z-0082-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "80845",
      "termination_date": "20190627",
      "more_code_info": "",
      "recall_initiation_date": "20180712",
      "postal_code": "33004-2401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}