{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84531",
      "recalling_firm": "Suntech Medical, Inc.",
      "address_1": "507 Airport Blvd Ste 117",
      "address_2": "",
      "postal_code": "27560-8200",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "No US Distribution; Internationally distributed to France, S. America",
      "recall_number": "Z-0810-2020",
      "product_description": "Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands:  Bravo Mini, part number 99-0233-00; Agilis Mini, part number NJ124 (99-0233-40); and NBP One, part number NBP One (99-0233-10).",
      "product_quantity": "384 units",
      "reason_for_recall": "The Bravo Mini (Model 250D), Agilis Mini (Model 250D), and NBP One (Model 250D) are being recalled because of a user safety issue when rechargeable batteries are misused in the product.",
      "recall_initiation_date": "20191211",
      "center_classification_date": "20200114",
      "termination_date": "20230410",
      "report_date": "20200122",
      "code_info": "All serial numbers.",
      "more_code_info": ""
    }
  ]
}