{
  "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": [
    {
      "country": "United States",
      "city": "Wayne",
      "address_1": "411 Newark Pompton Tpke",
      "reason_for_recall": "There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.",
      "address_2": "",
      "product_quantity": "85",
      "code_info": "Serial Numbers (each has \"A8WA-\" prefix): 00005  00076  00078  00079  00083  00011  00093  00036  00019  00122  00116  00117  00072  00038  00080  00115  00002  00013  00082  00010  00007  00089  00120  00121  00077  00084  00119  00146  00023  00021  00085  00112  00067  00124  00109  00107  00086  00009  00102  00104  00103  00071  00110  00028  00091  00060  00006  00008  00024  00014  00025  00081  00026  00027  00003  00075  00029  00098  00101  00097  00099  00022  00100  00087  00125  00032  00114  00073  00020  00001  00111  00088  00123  00063  00037  00030  00012  00062  00147  00118  00092  00065  00066  00113  00108",
      "center_classification_date": "20180327",
      "distribution_pattern": "Distributed in the following U.S. states: AL, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KY, LA, MA, MD,  MI, MN, MO, MS, NC, NJ, NM, NV, NY,  OH, OK, OR, PA, SC, TN, TX, UT, WA, WI and the District of Columbia. Distributed in Canada and Brazil.",
      "state": "NJ",
      "product_description": "Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8WA, UDI: 04560141944534",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Konica Minolta Medical Imaging USA, Inc.",
      "recall_number": "Z-1213-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79455",
      "termination_date": "20191028",
      "more_code_info": "",
      "recall_initiation_date": "20171204",
      "postal_code": "07470-6657",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}