{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25408",
      "product_res_number": "Z-0690-03",
      "event_date_initiated": "2002-12-11",
      "event_date_posted": "2003-03-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-06-02",
      "res_event_number": "25220",
      "product_code": "91",
      "k_numbers": [
        "K833113"
      ],
      "product_description": "ADx Tricyclic Antidepressants Reagent.  \nDistributed under the following label:\nADx, Abbott Laboratories USA, North Chicago, IL 60064",
      "code_info": "List no. 9681-55",
      "firm_fei_number": "2623532",
      "recalling_firm": "Abbott Health Products, Inc.",
      "address_1": "Hwy 2 Km 58.0",
      "city": "Barceloneta",
      "postal_code": "00617",
      "country": "PR",
      "additional_info_contact": "Nydia I. Cancel\n787-846-8256",
      "reason_for_recall": "Unexpected false positive TCA results",
      "root_cause_description": "Other",
      "action": "A Device Correction letter was mail to all customers on 12 /11/02. The letter explained the reason for the recall and provided specific instructions.",
      "distribution_pattern": "Distribution was nationwide, VA/DOD accounts. The   foreign distribution was as follows: Mexico, Venezuela, Colombia, Chile, Uruguay, Argentina, Brazil, Canada, England, Japan, Singapore, Hong Kong,  Taiwan, Thailand, Costa Rica, New Zealand and Panama",
      "openfda": {}
    }
  ]
}