{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "196753",
      "product_res_number": "Z-0339-2023",
      "event_date_initiated": "2022-10-10",
      "event_date_posted": "2022-12-02",
      "recall_status": "Terminated",
      "event_date_terminated": "2024-08-19",
      "res_event_number": "90999",
      "product_code": "BYJ",
      "k_numbers": [
        "K800742"
      ],
      "product_description": "CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit",
      "code_info": "UDI/DI M766133374030M766132561950, Serial Numbers:  CBB3022320073, CBB3022320077, CBB3022320074",
      "firm_fei_number": "3004972304",
      "recalling_firm": "Caire, Inc.",
      "address_1": "2200 Airport Industrial Dr Ste 500 2200 Airport Industrial Dr",
      "address_2": "Ste 500",
      "city": "Ball Ground",
      "state": "GA",
      "postal_code": "30107-4686",
      "additional_info_contact": "Sheril Ray\n770-721-7719",
      "reason_for_recall": "An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.",
      "root_cause_description": "Process control",
      "action": "The firm issued an URGENT:  MEDICAL DEVICE RECALL notice its consignees be email and telephone.  The notice explained the issue and requested the removal of the affected products from the field and return to CAIRE.  \n\nCAIRE will immediately replace the above serial numbers with new Liberator devices. Please contact CAIRE Customer Service via phone at 1-800-482-2473 or 770-721-7700 or via email at customerservice.usa@caireinc.com to arrange for the return and replacement of the above serial numbers.",
      "product_quantity": "3 units",
      "distribution_pattern": "US Nationwide - Worldwide Distribution:  CA, NC, OH, AZ, and Canada, Chile, Colombia, and Germany",
      "openfda": {
        "k_number": [
          "K971545",
          "K895082",
          "K032143",
          "K833994",
          "K863978",
          "K130068",
          "K853083",
          "K963956",
          "K863205",
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          "K041122",
          "K101272",
          "K103324",
          "K033000",
          "K072723",
          "K013251",
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          "K861503",
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          "K903140",
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          "K880183",
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          "K834290",
          "K882328",
          "K800742",
          "K830498",
          "K791902",
          "K993220",
          "K832143",
          "K880101",
          "K820836",
          "K080023",
          "K113767",
          "K864280",
          "K811162"
        ],
        "registration_number": [
          "3004972304",
          "3013156250",
          "1937980",
          "3009128734"
        ],
        "fei_number": [
          "3004972304",
          "2129616",
          "3013156250",
          "1937980"
        ],
        "device_name": "Unit, Liquid-Oxygen, Portable",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5655",
        "device_class": "2"
      }
    }
  ]
}