{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Eagan",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84883",
      "recalling_firm": "Braemar Manufacturing, LLC",
      "address_1": "1285 Corporate Center Dr Ste 150",
      "address_2": "",
      "postal_code": "55121-1278",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide.  No governmental consignees or Canadian consignees.  International distribution to Germany, Spain, Switzerland, France, Finland, Vietnam, Israel, France, Hong Kong, Czech Republic, Finland, Belgium, Sweden, Mexico, Lebanon, United Arab Emirates, Bolivia, Italy, and Belgium.",
      "recall_number": "Z-1459-2020",
      "product_description": "Braemar Manufacturing LLC  DL900 Holter Monitor  1285 Corporate Center Dr.  Suite 150  Eagan, MN 55121 USA  Rx Only",
      "product_quantity": "10582",
      "reason_for_recall": "An issue with the DL900 and DL950 Series Holter Recorder was recognized on January 1, 2020. This issue can prevent the recorder from operating normally.  Braemar confirmed that   beginning on January 1, 2020   if a AAA battery is inserted in the recorder and a user attempts to start it, the recorder will display  Error: 602  and fail to function for a new patient study. There are no actions that a clinical user can take to clear this  error. Even if this error code is displayed, existing ECG recordings stored on the device can still be downloaded via the standard Holter Application Software.  Error 602 may be able to be cleared by technical or engineering staff at the customer site.",
      "recall_initiation_date": "20200122",
      "center_classification_date": "20200310",
      "termination_date": "20220527",
      "report_date": "20200318",
      "code_info": "All devices manufactured or distributed prior to 01/01/2020 are affected.",
      "more_code_info": ""
    }
  ]
}