{
  "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,
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  "results": [
    {
      "cfres_id": "142305",
      "product_res_number": "Z-0603-2016",
      "event_date_initiated": "2015-11-20",
      "event_date_created": "2016-01-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2016-10-27",
      "res_event_number": "72825",
      "product_code": "LGZ",
      "k_numbers": [
        "K111870"
      ],
      "product_description": "AMSCO Warming Cabinet. Manufactured by: STERIS Corporation \n\nTo raise the temperature of blankets, linens and sterile surgical IV/irrigation solutions to an acceptable level for various surgical, obstetrical, emergency, critical care and other healthcare applications.",
      "code_info": "Serial #'s: 0428014026 - 0432115014",
      "firm_fei_number": "1527821",
      "recalling_firm": "Steris Corporation",
      "address_1": "5960 Heisley Rd",
      "city": "Mentor",
      "state": "OH",
      "postal_code": "44060-1834",
      "additional_info_contact": "Ms. Kathryn E. Cadorette\n440-392-7231",
      "reason_for_recall": "The firm discovered that information printed on the quick reference magnet is incorrect; specifically, Fahrenheit to Celsius temperature conversions and the default Warming Cabinet temperature.",
      "root_cause_description": "Process change control",
      "action": "The firm, Steris, sent an \"URGENT VOLUNTARY FIELD CORRECTION NOTICE\" letter dated 12/14/2015 to its customers. The letter described the product, problem and actions to be taken.  The firm included an updated quick reference magnet for each affected unit with the letter. The customers were instructed to replace your existing magnet with the enclosed magnet. \n\nIf you have questions regarding this matter, please contact Product Manager, at 440-392-7705 or STERIS Customer Service at 1-800-548-4873.",
      "product_quantity": "2,319 units",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Australia, Austria, Bahrain, Canada, China, Colombia, Costa Rica, France, Hong Kong, India, Indonesia, Israel, Kuwait, Lebanon, Mexico, Panama, Peru, Republic of Korea, Russian Federation, Saudi Arabia, Singapore, Spain, Taiwan, Thailand, Turkey, Uganda, United Arab Emirates, Viet Nam & Virgin Islands.",
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        "device_name": "Warmer, Thermal, Infusion Fluid",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
      }
    }
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}