{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "175288",
      "product_res_number": "Z-0017-2020",
      "event_date_initiated": "2019-06-27",
      "event_date_posted": "2019-10-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2021-08-10",
      "res_event_number": "83435",
      "product_code": "KJJ",
      "k_numbers": [
        "K082470"
      ],
      "product_description": "Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850",
      "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",
      "firm_fei_number": "3000209941",
      "recalling_firm": "Inter-Med Llc",
      "address_1": "2200 Northwestern Ave",
      "city": "Racine",
      "state": "WI",
      "postal_code": "53404-2500",
      "additional_info_contact": "Katy Scott\n414-639-9755",
      "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.",
      "root_cause_description": "Process control",
      "action": "The firm initiated the recall by letter on 06/27/2019. The letter directed the consignee to quarantine the product and contact the returns department for return instructions.",
      "product_quantity": "384 units",
      "distribution_pattern": "US, South Africa, Switzerland, Poland, Italy, Singapore, Australia",
      "openfda": {
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        "device_name": "Cleanser, Root Canal",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "U",
        "registration_number": [
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