{
  "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": "88",
      "code_info": "Serial Numbers (each has \"A7AP-\" prefix): 00045  00041  00004  00076  00090  00016  00037  00038  00060  00059  00091  00028  00089  00080  00077  00039  00057  00040  00007  00043  00024  00071  00003  00064  00011  00052  00027  00006  00044  00042  00063  00078  00087  00047  00031  00048  00008  00068  00095  00103  00096  00098  00097  00099  00100  00101  00102  00082  00084  00092  00083  00069  00079  00061  00019  00072  00081  00051  00018  00017  00065  00055  00053  00012  00015  00073  00023  00074  00002  00075  00066  00094  00020  00070  00056  00049  00025  00085  00093  00046  00086  00022  00009  00010  00021  00013  00014  00029",
      "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: A7AP, UDI: 04560141940031",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Konica Minolta Medical Imaging USA, Inc.",
      "recall_number": "Z-1212-2018",
      "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"
    }
  ]
}