{
  "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": "175202",
      "product_res_number": "Z-0011-2020",
      "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 CanalClean Endodontic Irrigation Kit, (1) 12mL - Chlor-XTRA, 6mL - SmearOFF + 92) + (2) 30ga Irrigation Tips + (1) Micro Aspirator with Tip, REF 504700",
      "code_info": "No UDI Lot/Work Order Numbers: 2018-1192 2018-1473 2018-1742 2018-1999 2018-2386 2018-2741 2019-0047",
      "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": "377 units",
      "distribution_pattern": "US, South Africa, Switzerland, Poland, Italy, Singapore, Australia",
      "openfda": {
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          "K173163",
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          "K061689",
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          "K211813",
          "K032627",
          "K201785",
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          "K802853",
          "K241354"
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        "device_name": "Cleanser, Root Canal",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "U",
        "registration_number": [
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