{
  "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,
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  },
  "results": [
    {
      "cfres_id": "27179",
      "product_res_number": "Z-0830-03",
      "event_date_initiated": "2003-04-23",
      "event_date_posted": "2003-05-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-02-05",
      "res_event_number": "26151",
      "product_code": "MLR",
      "product_description": "C1140 Flexible Endoscope Processing Container and Tray assembly.",
      "code_info": "Serial Numbers:  203793 - 204362",
      "firm_fei_number": "1527821",
      "recalling_firm": "Steris Corp",
      "address_1": "5960 Heisley Rd",
      "city": "Mentor",
      "state": "OH",
      "postal_code": "44060",
      "reason_for_recall": "The container flow port is inverted, which restricts the flow of sterilant to the endoscope and affects the sterilization process.",
      "root_cause_description": "Other",
      "action": "The firm notified their customers by telephone and letter on 4/23/2003.",
      "product_quantity": "354 units",
      "distribution_pattern": "The product was shipped to end-users located nationwide and worldwide.",
      "openfda": {
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        "device_name": "Sterilizer, Chemical",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6860",
        "device_class": "2"
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    }
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}