{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Carpinteria",
      "address_1": "1170 Mark Ave",
      "reason_for_recall": "To correct the kit's instructions for use as the storage time for gastric and gastroesophageal junction adenocarcinoma cut sections will be changed from six months to five months.",
      "address_2": "",
      "product_quantity": "1051 kits",
      "code_info": "Code No SK006  Lot #'s: 10127731A, 10126716C, 10127741, 10129051 and 10132199",
      "center_classification_date": "20180711",
      "distribution_pattern": "AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, NH, NJ, NV, NY, OH, OK, PA, TX, UT, VA, WA, and WI",
      "state": "CA",
      "product_description": "PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment options.",
      "report_date": "20180718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Dako North America Inc.",
      "recall_number": "Z-2425-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79602",
      "termination_date": "20201110",
      "more_code_info": "",
      "recall_initiation_date": "20180202",
      "postal_code": "93013-2918",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}