{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "44150",
      "product_res_number": "Z-0574-06",
      "event_date_initiated": "2006-02-10",
      "event_date_posted": "2006-02-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-06-23",
      "res_event_number": "34590",
      "product_code": "LFW",
      "k_numbers": [
        "K912143"
      ],
      "product_description": "Roche brand CEDIA Tobramycin II Reagent, Catalog # 1815385, Material # 11815385216.",
      "code_info": "Lot 56292625; exp. 05/31/07.",
      "firm_fei_number": "1823260",
      "recalling_firm": "Roche Diagnostics Corp.",
      "address_1": "9115 Hague Rd",
      "city": "Indianapolis",
      "state": "IN",
      "postal_code": "46256-1025",
      "additional_info_contact": "800-428-2336",
      "reason_for_recall": "May have tobramycin over-recovery at the trough level.",
      "root_cause_description": "Other",
      "action": "Consignees were notified via phone and faxed recall letter on or about 2/10/06.",
      "product_quantity": "1806 kits",
      "distribution_pattern": "Nationwide.",
      "openfda": {
        "k_number": [
          "K843828",
          "K944371",
          "K900707",
          "K964670",
          "K854392",
          "K941614",
          "K894531",
          "K872562",
          "K841866",
          "K912143"
        ],
        "registration_number": [
          "9610126",
          "3010939897"
        ],
        "fei_number": [
          "3002806559",
          "3010939897"
        ],
        "device_name": "Fluorescence Polarization Immunoassay, Tobramycin",
        "medical_specialty_description": "Clinical Toxicology",
        "regulation_number": "862.3900",
        "device_class": "2"
      }
    }
  ]
}