{
  "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": "42419",
      "product_res_number": "Z-0136-06",
      "event_date_initiated": "2005-09-30",
      "event_date_posted": "2005-11-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-16",
      "res_event_number": "33774",
      "product_code": "GGT",
      "product_description": "Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512",
      "code_info": "Kit lots# 63-502081, 63-502081A contain Calibration Verifiers 1, 2, and 3. Lot #30-500952 is specific to Calibration Verifier 2; Lot #30-500953 is specific to Calibration Verifier 3.",
      "firm_fei_number": "2050095",
      "recalling_firm": "Nichols Institute Diagnostics",
      "address_1": "1311 Calle Batido",
      "city": "San Clemente",
      "state": "CA",
      "postal_code": "92673-6316",
      "additional_info_contact": "John Chiechi\n949-940-7377",
      "reason_for_recall": "Some units in Lot 30-500953 (Calibration Verifier 2) are mislabeled as Calibration Verifier 3. Some units of Lot 30-500953 (Calibration Verifier 3) are mislabeled as Calibration Verifier 2.",
      "root_cause_description": "Other",
      "action": "Written notification was sent via fax on 9/29/05. If receipt was not confirmed, written version of notification was mailed via next day delivery. NID intends to track the response forms and if after 2 weeks after distribution not all forms have been received, NID will conduct a follow-up phone call and resend if necessary.",
      "product_quantity": "215",
      "distribution_pattern": "CA, IN, WA",
      "openfda": {
        "k_number": [
          "K980737",
          "K954898",
          "K931666",
          "K936016",
          "K992799",
          "K902639",
          "K932650",
          "K052223",
          "K894943",
          "K240182",
          "K983203",
          "K926390",
          "K893393",
          "K903492",
          "K183088",
          "K952559",
          "K910481",
          "K833957",
          "K931756",
          "K882686"
        ],
        "device_name": "Assay, Erythropoietin",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.7250",
        "device_class": "2",
        "registration_number": [
          "2432235",
          "2245285",
          "3002800697",
          "8032314",
          "2182501",
          "1222302",
          "2025099",
          "2122870",
          "3002806944"
        ],
        "fei_number": [
          "2432235",
          "2245285",
          "3002800697",
          "2182501",
          "3007981058",
          "3002806944",
          "1000121039",
          "2122870",
          "3002808140"
        ]
      }
    }
  ]
}