{
  "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-0015-2020",
      "product_description": "Vista Dental Products 3% Sodium Hypochlorite, 10- 3cc Pre-filled Syringes, REF 502355",
      "product_quantity": "445 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": "UDI (01)10818207020410  Lot/Work Order Numbers:  20182545  20182665  20190198  20190432  20190724  20190953  20191314"
    }
  ]
}