{
  "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": 55
    }
  },
  "results": [
    {
      "cfres_id": "53847",
      "product_res_number": "Z-0006-2008",
      "event_date_initiated": "2007-07-24",
      "event_date_posted": "2007-10-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-10-16",
      "res_event_number": "38484",
      "product_code": "BSF",
      "product_description": "GE Disposable Multi Absorber Canister used with EZchange Module for the  Aisys, Avance,  Aespire Anesthesia systems. The EZchange Module is an optional accessory for these anesthesia systems.",
      "code_info": "EZchange Manifold with part number 1407-7021-000,  1407-7027-000, M1053007, M1053008.",
      "firm_fei_number": "2183066",
      "recalling_firm": "Datex - Ohmeda, Inc",
      "address_1": "Po Box 7550",
      "address_2": "Po Box 7550",
      "city": "Madison",
      "state": "WI",
      "postal_code": "53707",
      "reason_for_recall": "Elevated inspired CO2 levels related to the use of the Datex-Ohmeda GE Healthcare Disposable Multi Absorber Canister with the EZchange Module.",
      "root_cause_description": "Vendor change control",
      "action": "Because this issue only occurs when the Disposable Multi Absorber is used in conjunction with EZchange Module, they have contacted all EZchange Module customers.  It is critical to contact these customers specifically, rather than all customers shipped Disposable Multi Absorbers as this may cause unwarranted confusion with customers who do not have the EZchange Module.  Consignees were sent an letter dated 7/19/2007  describing the product and problem. The letter lists a number of interim actions to implement with the anesthesia systems.",
      "product_quantity": "389,070",
      "distribution_pattern": "Worldwide, including USA, Australia, Belgium, Brazil, Canada, Chile, China, Denmark, Egypt, Estonia, Finland, France, Germany, India, Ireland, Italy, Jordan, Republic of Korea, Kuwait, Mexico, Netherlands, New Zealand, Norway, Peru, Poland, Qatar, Singapore, Slovak Republic, South Africa, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom, and Venezuela.",
      "openfda": {
        "device_name": "Absorber, Carbon-Dioxide",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5310",
        "device_class": "1",
        "k_number": [
          "K852071",
          "K951093",
          "K760076",
          "K821144",
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          "K833452",
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        ],
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