{
  "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,
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  "results": [
    {
      "cfres_id": "25592",
      "product_res_number": "Z-0557-03",
      "event_date_initiated": "2002-12-18",
      "event_date_posted": "2003-02-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-04-14",
      "res_event_number": "25319",
      "k_numbers": [
        "K013899"
      ],
      "product_description": "CARTON LABEL: ''TDM Performance Verifier I'';  6 x 2 mL vials **** Catalog Number 896 2540 ****  Made in USA by Ortho-Clinical Diagnostics , Inc., 100 Indigo Creek Drive, Rochester, NY  14626 ****",
      "code_info": "T3606, Exp 31 Mar 2004",
      "firm_fei_number": "1000136573",
      "recalling_firm": "Ortho-Clinical Diagnostics",
      "address_1": "100 Indigo Creek Drive",
      "city": "Rochester",
      "state": "NY",
      "postal_code": "14650-0881",
      "additional_info_contact": "Sherry L. Phillips\n585-453-3728",
      "reason_for_recall": "Cartons labeled 'TDM Performance Verifier I' may contain TDM Performance Verified II.",
      "root_cause_description": "Other",
      "action": "Letters dated 12/18/02 with instructions to inspect inventory and to discard affected product.",
      "product_quantity": "1,338 cartons",
      "distribution_pattern": "Nationwide distribution to medical facilities, distributors, and U.S. government consignees (39).",
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}