{
  "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": [
    {
      "status": "Terminated",
      "city": "Racine",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83435",
      "recalling_firm": "Inter-Med Llc",
      "address_1": "2200 Northwestern Ave",
      "address_2": "N/A",
      "postal_code": "53404-2500",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US, South Africa, Switzerland, Poland, Italy, Singapore, Australia",
      "recall_number": "Z-0017-2020",
      "product_description": "Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850",
      "product_quantity": "384 units",
      "reason_for_recall": "The affected lots may be packaged in syringes which include an incorrect bung.  The incorrect bung is made of a latex-free isoprene rubber material.  After prolonged storage and exposure to contained solutions, the rubber bung may degrade due to chemical interaction with the bleach solution.",
      "recall_initiation_date": "20190627",
      "center_classification_date": "20191001",
      "termination_date": "20210810",
      "report_date": "20191009",
      "code_info": "Lot/Work Order Numbers:  2018-1471  2018-1992  20182211, UDI (01)10818207020502  20182779, UDI (01)10818207020502  20190041, UDI (01)10818207020502  20190309, UDI (01)10818207020502"
    }
  ]
}