{
  "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": "Carpinteria",
      "address_1": "6392 Via Real",
      "reason_for_recall": "Dako is recalling the PT Link Waterbath because of a possible electrical hazard.   Specifically, if the heater pad under the reagent tank becomes wet, it may present an electrical shock hazard when the lid is open.",
      "address_2": "",
      "product_quantity": "136 units",
      "code_info": "Catalog #: PT-Module",
      "center_classification_date": "20121113",
      "distribution_pattern": "Nationwide distribution: USA including states of: AK, CA, CO,  CT, DC, FL, GA, HI, IA, IL IN, KS, KY, MA, MD, MI, MN, MO, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, and WA.",
      "state": "CA",
      "product_description": "PT Link Waterbath, Model#PT100.    Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.",
      "report_date": "20121121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Dako North America Inc.",
      "recall_number": "Z-0287-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "53336",
      "termination_date": "20121113",
      "more_code_info": "",
      "recall_initiation_date": "20080501",
      "postal_code": "93013-2921",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}