{
  "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": [
    {
      "status": "Terminated",
      "city": "Sanford",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64718",
      "recalling_firm": "Separation Technology, Inc.",
      "address_1": "582 Monroe Rd Ste 1424",
      "address_2": "N/A",
      "postal_code": "32771-8821",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of PA, NC, IL, KS, and FL, and the countries Canada and Turkey.",
      "recall_number": "Z-1367-2013",
      "product_description": "SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE.    Produce a monolayer of cells onto a glass slide from any fluid suspension.",
      "product_quantity": "102",
      "reason_for_recall": "Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges manufactured prior to January 1, 2013 for having the potential to start up unexpectedly when encountering an electrostatic discharge.",
      "recall_initiation_date": "20130313",
      "center_classification_date": "20130523",
      "termination_date": "20131224",
      "report_date": "20130529",
      "code_info": "Serial numbers: 0110, 0111, 0112, 0210, 0211, 0212, 0310, 0311, 0312, 0410, 0411, 0412, 0511, 0512, 0611, 0710, 0711, 0811, 0812, 0910, 0911, 0912, 1011, 1012, 1112, 1210, 1212."
    }
  ]
}