{
  "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": "2026-08-13",
    "results": {
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      "product_res_number": "Z-0283-04",
      "event_date_initiated": "2004-02-06",
      "event_date_posted": "2004-07-20",
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      "res_event_number": "28191",
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      "recalling_firm": "General Electric Med Systems",
      "address_1": "3000 N Grandview Blvd",
      "city": "Waukesha",
      "state": "WI",
      "postal_code": "53188-1615",
      "additional_info_contact": "Larry A. Kroger\n262-544-3894",
      "reason_for_recall": "The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam and the technical specification for the maximum line current.",
      "root_cause_description": "Other",
      "action": "The consignees were sent 'Regulatory Notice' letters dated February 6, 2004.  The letters informed the consignees of the violations and provided them with the technical specifications which needed to be provided.",
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