{
  "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
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  },
  "results": [
    {
      "cfres_id": "26111",
      "product_res_number": "Z-0616-03",
      "event_date_initiated": "2003-02-07",
      "event_date_posted": "2003-03-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-05-02",
      "res_event_number": "25589",
      "product_code": "LJC",
      "k_numbers": [
        "K951010"
      ],
      "product_description": "Chlamydia OIA. For in vitro diagnostic use.",
      "code_info": "Catalog No. CHLINT, Lot No. 133354, 133174. Foreign distribution.",
      "firm_fei_number": "1720655",
      "recalling_firm": "Thermo Biostar, Incorporated",
      "address_1": "331 South 104th Street",
      "city": "Louisville",
      "state": "CO",
      "postal_code": "80027",
      "reason_for_recall": "Chlamydia IVD test kits may contain diluted conjugate reagent. Use may produce a false negative result with a low positive patient sample.",
      "root_cause_description": "Other",
      "action": "All consignees were notified by telephone on 2/6/2003, followed by letter on 2/10/2003.",
      "product_quantity": "56 units",
      "distribution_pattern": "Nationwide, and to France, New Zealand and Spain.",
      "openfda": {
        "k_number": [
          "K982210",
          "K901934",
          "K921462",
          "K895468",
          "K960850",
          "K861966",
          "K895505",
          "K900402",
          "K862638",
          "K883266",
          "K910668",
          "K946276",
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          "K880783",
          "K893676",
          "K863490",
          "K921321",
          "K902270",
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          "K951010",
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          "K864842",
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          "K862948",
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          "K892371",
          "K831962",
          "K882535",
          "K940564",
          "K895122",
          "K926090",
          "K033865",
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          "K920503",
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          "K880799",
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          "K872056",
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          "K884517",
          "K905179",
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          "K955627",
          "K033079",
          "K882676",
          "K935393",
          "K821967",
          "K901660",
          "K903758"
        ],
        "registration_number": [
          "3043226252",
          "3022178699",
          "3002792284",
          "2029372",
          "3003750284",
          "3005360469",
          "1318354",
          "3012494290",
          "3033507883",
          "8030124"
        ],
        "fei_number": [
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          "3005670738",
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          "3002792284",
          "3003750284",
          "3003206361",
          "1318354",
          "3012494290",
          "3033507883",
          "1000306617"
        ],
        "device_name": "Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3120",
        "device_class": "1"
      }
    }
  ]
}