{
  "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": "75 units",
      "code_info": "Serial No.  ACBE20120900183  ACBE20120900189  ACBE20120900205  ACBE20120900206  ACBE20121000217  ACBE20121000224  ACBE20121000225  ACBE20121000226  ACBE20121000231  ACBE20121000232  ACBE20121000236  ACBE20121000240  ACBE20121000245  ACBE20121000250  ACBE20121000252  ACBE20121000259  ACBE20121000260  ACBE20121000261  ACBE20121000262  ACBE20121000271  ACBE20121100292  ACBE20121100296  ACBE20121100300  ACBE20130200445  ACBE20120900211  ACBE20121000222  ACBE20121000237  ACBE20121000246  ACBE20121000263  ACBE20121100277  ACBE20121100280  ACBE20121100283  ACBE20121100287  ACBE20121100291  ACBE20121100356  ACBE20121100360  ACBE20121100364  ACBE20130100394  ACBE20130100395  ACBE20130100397  ACBE20130100398  ACBE20130100399  ACBE20130100401  ACBE20130100402  ACBE20130100404  ACBE20130100405  ACBE20130100410  ACBE20130100411  ACBE20130100412  ACBE20130100415  ACBE20130100417  ACBE20121000218  ACBE20121000227  ACBE20121000270  ACBE20121100282  ACBE20121100286  ACBE20121100288  ACBE20121100301  ACBE20121100350  ACBE20121100352  ACBE20121100355  ACBE20130100369  ACBE20130100370  ACBE20130100374  ACBE20130100375  ACBE20130100376  ACBE20130100378  ACBE20130100379  ACBE20130100380  ACBE20130100384  ACBE20130100385  ACBE20130100388  ACBE20130100390  ACBE20130100392  ACBE20130100393",
      "center_classification_date": "20130729",
      "distribution_pattern": "US distribution including CA and UT.",
      "state": "CA",
      "product_description": "ViSi Mobile Chest Sensor (3 lead-wire ECG, AAMI), Catalog No. 93-10014    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-1818-2013",
      "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"
    }
  ]
}