{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "9444 Waples St",
      "reason_for_recall": "Sotera Wireless, Inc. is recalling the ViSi Mobile Monitoring System due to the potential for the Chest Sensor to cause a blister wound.",
      "address_2": "#280",
      "product_quantity": "90 units",
      "code_info": "Serial No.  AAAA20120800519  AAAA20120800520  AAAA20120800526  AAAA20120800527  AAAA20120800533  AAAA20120800537  AAAA20120800538  AAAA20120800539  AAAA20120900544  AAAA20120900548  AAAA20120900557  AAAA20120900562  AAAA20120900564  AAAA20120900577  AAAA20120900578  AAAA20120900580  AAAA20120900584  AAAA20120900587  AAAA20120900591  AAAA20130400890  AAAA20130400896  AAAA20130400902  AAAA20130400909  AAAA20120800501  AAAA20121200604  AAAA20121200606  AAAA20121200609  AAAA20121200610  AAAA20121200611  AAAA20121200615  AAAA20121200617  AAAA20121200618  AAAA20121200620  AAAA20121200621  AAAA20121200624  AAAA20121200626  AAAA20121200628  AAAA20121200629  AAAA20121200630  AAAA20121200632  AAAA20121200636  AAAA20121200639  AAAA20121200640  AAAA20121200645  AAAA20121200647  AAAA20130100680  AAAA20130100684  AAAA20130100688  AAAA20130100689  AAAA20130100691  AAAA20130100692  AAAA20130100693  AAAA20130100694  AAAA20130100698  AAAA20130100699  AAAA20130100700  AAAA20130100701  AAAA20130100703  AAAA20121200605  AAAA20121200612  AAAA20121200613  AAAA20121200622  AAAA20121200625  AAAA20121200627  AAAA20121200633  AAAA20121200642  AAAA20121200643  AAAA20121200646  AAAA20121200648  AAAA20121200649  AAAA20121200650  AAAA20121200651  AAAA20121200652  AAAA20121200653  AAAA20130100654  AAAA20130100655  AAAA20130100656  AAAA20130100657  AAAA20130100658  AAAA20130100660  AAAA20130100661  AAAA20130100662  AAAA20130100664  AAAA20130100665  AAAA20130100666  AAAA20130100669  AAAA20130100670  AAAA20130100671  AAAA20130100672  AAAA20130100678",
      "center_classification_date": "20130729",
      "distribution_pattern": "US distribution including CA and UT.",
      "state": "CA",
      "product_description": "ViSi Mobile Monitor, Catalog No. 92-10010    The ViSi Mobile Monitoring System is intended for use by clinicians and medically qualified personnel for single or multi-parameter vital signs monitoring of adult patients.",
      "report_date": "20130807",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sotera Wireless, Inc.",
      "recall_number": "Z-1817-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65718",
      "termination_date": "20130909",
      "more_code_info": "",
      "recall_initiation_date": "20130523",
      "postal_code": "92121-2939",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}