{
  "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",
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      "event_date_initiated": "2022-11-30",
      "event_date_posted": "2023-01-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-08-31",
      "res_event_number": "91335",
      "product_code": "INN",
      "product_description": "ActiveAid 922, Shower/Commode Chair",
      "code_info": "Serial Number 90071504001",
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      "recalling_firm": "Altimate Medical, Inc.",
      "address_1": "262 W 1st St",
      "city": "Morton",
      "state": "MN",
      "postal_code": "56270-1179",
      "additional_info_contact": "Amy Curtis\n507-697-6393",
      "reason_for_recall": "Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.",
      "root_cause_description": "Component change control",
      "action": "Altimate Medical notified its sole consignee by telephone on 11/30/2022 and followed with an Urgent Medical Device Recall letter on 12/06/2022.  The notice stated the problem and requested the following action:\n\"- Acknowledge receipt of this notification.  Complete and return the attached Acknowledgement form.\n- Inform the customer not to use the chair if this has not already done.\n- Provide replacement chair 90071504001 under RMA000737 to AMI\n- Inform Altimate when the replacement chair is provided to the customer.  Complete and return the attached Verification form.\"",
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