{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "189465",
      "product_res_number": "Z-0161-2022",
      "event_date_initiated": "2021-09-10",
      "event_date_created": "2021-10-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2025-08-27",
      "res_event_number": "88760",
      "product_code": "IKZ",
      "product_description": "Easi-Care Gait Belt Metal Buckle (54\", 60\", and 72\" lengths)",
      "code_info": "Kinsman Product Numbers: 80805 (54\"), 80806 (60\"), and 80807 (72\")\n\nUPC codes: 873704007275, 873704006773, 873704007282",
      "firm_fei_number": "1000570634",
      "recalling_firm": "Kinsman Enterprises Inc",
      "address_1": "10804 Mark Twain Rd",
      "city": "W Frankfort",
      "state": "IL",
      "postal_code": "62896-4105",
      "additional_info_contact": "618-932-3838",
      "reason_for_recall": "The belt may fail at lower loads than the labeled 600lbs.",
      "root_cause_description": "Component change control",
      "action": "The recalling firm sent recall notification via email beginning 09/23/2021.  The scope of the recall includes all product (Items 80805, 80806, and 80807) shipped between May 17, 2021 and August 11, 2021.  Customers are asked to immediately check stock and quarantine any impacted product.  Impacted product is not to be used.  Recalled devices must be returned to the recalling firm and will be replaced.  A Verification Form should be completed and returned via email to recall@kinsmanenterprises.com.  Distributors must promptly notify any potentially impacted customers to which they have further distributed product.",
      "product_quantity": "13,123 units",
      "distribution_pattern": "Distribution in CA, FL, GA, IL, KY, MI, MS, NC, NH, NJ, NY, OH, TN, VA",
      "openfda": {
        "k_number": [
          "K922473",
          "K950681",
          "K972486",
          "K954671",
          "K822402",
          "K842604",
          "K933964",
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          "K962788",
          "K905390",
          "K923710",
          "K810220",
          "K823095",
          "K950756",
          "K834563"
        ],
        "device_name": "Bed, Patient Rotation, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5225",
        "device_class": "2",
        "registration_number": [
          "3015423385",
          "3016947689",
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}