{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "30369",
      "product_res_number": "Z-0210-04",
      "event_date_initiated": "2003-11-07",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-02-24",
      "res_event_number": "27695",
      "product_code": "NEP",
      "k_numbers": [
        "K002705"
      ],
      "product_description": "Exacta-Mix 2400 pharmacy compounding system.",
      "code_info": "Catalog Number EM2400, all serial numbers.",
      "firm_fei_number": "1419106",
      "recalling_firm": "Baxa Corporation",
      "address_1": "14445 Grasslands Dr",
      "city": "Englewood",
      "state": "CO",
      "postal_code": "80112-7062",
      "additional_info_contact": "303-617-2181",
      "reason_for_recall": "If device stops due to an alarm or operater pause, inlet valves will remain open, allowing some unwanted mixing of ingredients in the valve chamber..",
      "root_cause_description": "Other",
      "action": "All users were contacted by phone and fax on 11/7/03 with instructions to safely use the device.",
      "product_quantity": "231 systems",
      "distribution_pattern": "Nationwide. Foreign distribution to UK. No government or military consignees.",
      "openfda": {
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        "device_name": "System/Device, Pharmacy Compounding",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5440",
        "device_class": "2"
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    }
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}