{
  "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": "Burlington",
      "address_1": "780 Plantation Dr",
      "reason_for_recall": "Some Prep Stain Kit, 1.2 DiTi Cones have been found to be leaking and the PrepStain Preparation kits contain incorrect preventive maintenance (PM) instructions.",
      "address_2": "",
      "product_quantity": "1274 units",
      "code_info": "Catalog # 491074: Serial/Lot # 110805MA",
      "center_classification_date": "20120726",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including Puerto Rico and the states  AL, AK, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY, and WV and  the countries of  Belgium, Brazil, Canada, China, Columbia, Hong Kong, India, Japan, Korea, Peru, Singapore, Taiwan and Victoria (Australia).",
      "state": "NC",
      "product_description": "PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone.    The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain System produces SurePath Slides that are intended for use in the screening and detection of cervical cancer, pre-cancerous lesions, atypical cells and all other cytologic categories as defined by The Bethesda System for Reporting Cervical/Vaginal Cytology Diagnoses. The 1.2 DiTi is the tip on the PrepStain to which a pipette tip attaches and dispenses patient samples onto a glass microscope slide.",
      "report_date": "20120801",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tripath Imaging, Inc.",
      "recall_number": "Z-2086-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62117",
      "termination_date": "20131108",
      "more_code_info": "",
      "recall_initiation_date": "20111208",
      "postal_code": "27215-6723",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}