{
  "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": "43401",
      "product_res_number": "Z-0382-06",
      "event_date_initiated": "2005-12-07",
      "event_date_posted": "2006-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-02-26",
      "res_event_number": "34273",
      "product_code": "LTJ",
      "pma_numbers": [
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      "code_info": "Lot 171735.",
      "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": "There is the possibility of high results with sera expected to have non-detectable levels of tPSA if these reagent lots are used in combination on the Modular Analytics E170 analyzer.",
      "root_cause_description": "Other",
      "action": "Consignees were notified of the incompatibility via reagent bulletin dated 12/7/05.",
      "product_quantity": "25,000 kits",
      "distribution_pattern": "Nationwide.",
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        "device_name": "Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers",
        "medical_specialty_description": "Immunology",
        "regulation_number": "866.6010",
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}