{
  "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": "203624",
      "product_res_number": "Z-0222-2024",
      "event_date_initiated": "2023-09-25",
      "event_date_posted": "2023-11-03",
      "recall_status": "Open, Classified",
      "res_event_number": "93188",
      "product_code": "IQA",
      "product_description": "Arial Water Resistant Pendant with Long Wristband, Models:  59362 and 2560-59362; mobile patient alarm",
      "code_info": "Manufacturing date codes:  23128 to 23251",
      "firm_fei_number": "1929691",
      "recalling_firm": "Securitas Healthcare LLC",
      "address_1": "4600 Vine St",
      "city": "Lincoln",
      "state": "NE",
      "postal_code": "68503-2823",
      "additional_info_contact": "Ameya Oke\n812-371-7115",
      "reason_for_recall": "Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.",
      "root_cause_description": "Component change control",
      "action": "Securitas Healthcare issued a recall notice to its consignees on 09/25/2023 via USPS, registered mail.  The notice explained the issue, potential hazard, and requested the following actions:\n1.\tImmediately replace Pendant battery upon Low Battery Alert\n2.\tCustomer should check Pendant battery status in Arial System application at least daily\n3.\tCustomer should check for Pendants that are no longer communicating with the Arial  System at least daily\n\nThis notice must be passed on to those who need to be aware within your organization.\n\n - Securitas Healthcare will be replacing all Pendants from the Affected Lots with refurbished Pendants at no cost. \n\nThe notice has also been posted:  https://www.securitashealthcare.com/product-advisories",
      "product_quantity": "49 devices",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "openfda": {
        "k_number": [
          "K902664",
          "K944585",
          "K953905",
          "K926029",
          "K872937",
          "K911101",
          "K940223",
          "K943244",
          "K901028",
          "K832057",
          "K881634",
          "K872936",
          "K890596",
          "K840808",
          "K921528",
          "K961306",
          "K850314",
          "K770028",
          "K900969",
          "K851740",
          "K953937",
          "K873612",
          "K944345",
          "K850313"
        ],
        "registration_number": [
          "3012505893",
          "3011699327",
          "3017404332",
          "3009591865",
          "1320360",
          "3030181825",
          "3007200970",
          "3008952681",
          "1929691",
          "3003114240",
          "3002713667",
          "3013513594",
          "3008855170",
          "3001757821",
          "3006802317",
          "3014024339",
          "3006789226",
          "3021667368"
        ],
        "fei_number": [
          "3012505893",
          "3011699327",
          "3017404332",
          "3009591865",
          "3030181825",
          "3007200970",
          "3008952681",
          "1929691",
          "3000210521",
          "3003114240",
          "3002713667",
          "3013513594",
          "3008855170",
          "3001757821",
          "3006802317",
          "3014024339",
          "3006789226",
          "3021667368"
        ],
        "device_name": "System, Environmental Control, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.3725",
        "device_class": "2"
      }
    }
  ]
}