{
  "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": "27751",
      "product_res_number": "Z-0174-04",
      "event_date_initiated": "2003-06-09",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-05-08",
      "res_event_number": "26479",
      "product_code": "LLI",
      "product_description": "Invacare IVC Home Care Bed (Foot Section with new head actuator from Linak.",
      "code_info": "Foot section model numbers and serial number ranges: Model #              Beginning S/N    Ending S/N 5490IVC            03D891256        03E035155 5890IVC            03D889942        03E002241 5491IVC            03E969254         03E433379 5891IVC            03E970154         03E971163  Bed Models that include the recalled food sections: 5310IVC, 5311IVC, 5410IVC, 5411IVC  Bed package model numbers which include the affected Beds and foot sections:  BED-21VC, BED-4IVC, BED-9IVC, BED-10IVC, BED-19IVC, BED-21IVC, BED-22IVC, BED-23IVC, BED-24IVC, BED-25IVC, BED-26IVC, BED-27IVC, BED-28IVC, BED-29IVC, BED-32IVC, BED-33IVC, BED-34IVC, BED-35IVC, BED-36IVC, BED-37IVC, CBED-2IVC, CBED-4IVC, CBED-4BIVC, CBED-11IVC, CBED-11BIVC, CBED-12IVC, CBED-12BIVC, CBED-19IVC, CBED-22IVC, CBED-23IVC, CBED-26IVC, CBED-28IVC.",
      "firm_fei_number": "3002889431",
      "recalling_firm": "Invacare Corporation",
      "address_1": "One Invacare Way",
      "city": "Elyria",
      "state": "OH",
      "postal_code": "44036",
      "additional_info_contact": "Stephen D. Neese\n800-333-6900",
      "reason_for_recall": "Pull tube on bed may bend or separate causing inoperability of bed or head section to fall.",
      "root_cause_description": "Other",
      "action": "The firm began telephoning direct consignees on 6/9/03 and also began sending recall letters to these consignees on 6/9/03.  The letter provides a list of affected units shipped to the consignee and the serial number of the affected foot section on the bed.  If the consignee indicated they wanted to perform the correction themselves then the indicated number of corrective bracket installation kits are being sent.  Also they are given the option of having an Invacare authorized service center perform the correction.  This is for units in their possession and also at patient homes. As of October 2003 enough corrective kits have been forwarded to dealers to correct all involved units.",
      "product_quantity": "5926",
      "distribution_pattern": "involved products were distributed to approximately 1100 dealers in the United Stated and to 54 Canadian dealer accounts.",
      "openfda": {
        "k_number": [
          "K022387",
          "K840787"
        ],
        "registration_number": [
          "3011719874",
          "3006891315",
          "3016678950",
          "3008951110",
          "3030488262",
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          "3010880685",
          "3006795832",
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          "3008466086",
          "3007689746",
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          "3034731542",
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          "3014615038",
          "3017171467",
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        ],
        "fei_number": [
          "3011719874",
          "3006891315",
          "3016678950",
          "3008951110",
          "3030488262",
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          "3003513125",
          "3038304894",
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          "3034731542",
          "3003751839",
          "3008058231",
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          "3015337241",
          "3017580820",
          "3008061384",
          "3014615038",
          "3017171467",
          "3008830652"
        ],
        "device_name": "Bed, Therapeutic, Ac-Powered, Adjustable Home-Use",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5100",
        "device_class": "2"
      }
    }
  ]
}