{
  "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": {
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  "results": [
    {
      "cfres_id": "122872",
      "product_res_number": "Z-0472-2014",
      "event_date_initiated": "2013-09-19",
      "event_date_posted": "2013-12-13",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-03-10",
      "res_event_number": "66638",
      "product_code": "BSF",
      "product_description": "Multi Absorber Original, Disposable\r\nM1173310 Multi Absorber Original, Disposable, package of 6 pcs,\r\n\r\nGE Healthcare Finland Oy\r\nMade in US\r\nRx Only\r\n\r\nThe GE Healthcare Multi Absorber Original, Disposable is a disposable product intended for use with the GE Healthcare Advanced Breathing System (later ABS), the GE Healthcare EZchange manifold, the GE Healthcare Compact Block, and the GE Healthcare Compact Block II (later Compact Block). The Multi Absorber should only be used with air, oxygen, nitrous oxide, halothane, enflurane, isoflurane, desflurane and sevoflurane. The device is intended to be used under constant attention of qualified professional healthcare personnel.",
      "code_info": "product number  M1173310 containing lot numbers 12001 through 13031.",
      "firm_fei_number": "2126677",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "city": "Waukesha",
      "state": "WI",
      "postal_code": "53188-1615",
      "additional_info_contact": "262-513-4122",
      "reason_for_recall": "GE Healthcare has recently become aware of a potential safety issue due to air leakage associated with the CO2 Multi Absorber.",
      "root_cause_description": "Device Design",
      "action": "GE issued an Urgent Medical Device Correction letter dated September 19, 2013, to all affected customers via Fed Ex overnight mail.  The letter identified the product, the problem, and the action to be taken by the customer.  Customers were instructed to not use the affected product, isolate all affected product and return the attached form via fax to 800-535-7923.  Once the information is received, customers would be contacted with an RMA and replacement information.  If product was distributed further  the notice should be forwarded to those customers.  For questions customers should call 1-800-345-2700, option 2 followed by ooption 2.  For foreign customers 1-800-932-0760, option 2.\r\nFor questions regarding this recall call 262-513-4122. GE issued a press release on 12/30/2013.",
      "product_quantity": "US: 59,721 boxes, 358,326 canisters; OUS: 3,724 boxes, 22,344 canisters",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) Puerto Rico and Internationally to Canada, Costa Rica, Mexico, and Venezuela.",
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          "K801255",
          "K951093",
          "K760076",
          "K852071",
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          "K834535",
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        ],
        "device_name": "Absorber, Carbon-Dioxide",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5310",
        "device_class": "1",
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