{
  "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": "30573",
      "product_res_number": "Z-0550-04",
      "event_date_initiated": "2003-11-24",
      "event_date_posted": "2004-02-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-02-07",
      "res_event_number": "27820",
      "product_description": "Clinical Chemistry Urea Nitrogen",
      "code_info": "Lots: 05073HW00 04022Hw00 03041HW00",
      "firm_fei_number": "2018433",
      "recalling_firm": "Abbott Laboratories Diagnostic Div",
      "address_1": "820 Mission St",
      "city": "South Pasadena",
      "state": "CA",
      "postal_code": "91030-3142",
      "additional_info_contact": "Linda Morris\n972-518-6711",
      "reason_for_recall": "Low results due to contaminant.",
      "root_cause_description": "Other",
      "action": "Each domestic customer will receive the recall letter by direct mailing. Foreign affiliates will be responsible for distributing letters to thier customers. Letters were sent 11/24/2003. A reply form was enclosed.",
      "product_quantity": "568",
      "distribution_pattern": "Nationwide, Mexico, Argentina, Germany, Australia, Venezuela, Puerto Rico, Singapore, New Zealand, Columbia, Canada, Hong Kong, Grand Cayman",
      "openfda": {}
    }
  ]
}