{
  "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": "Gaithersburg",
      "address_1": "1201 Clopper Rd",
      "reason_for_recall": "CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials.",
      "address_2": "",
      "product_quantity": "90 kits in total",
      "code_info": "Catalog Number 4503225, Lot #142345648, Exp: 06/09/14 & Lot #142357718  Exp: 06/09/14",
      "center_classification_date": "20130514",
      "distribution_pattern": "USA Nationwide Distribution including the states of: CA, DC, FL, GA, MA, MD, MI, and IL.",
      "state": "MD",
      "product_description": "QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225)     Product Usage:  Test is intended for use in the detection and quantitation of human cytomegalovirus (CMV) specific DNA, as part of an in house validated real-time PCR assay.  One service package containing the handbook.",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "QIAGEN Gaithersburg, Inc.",
      "recall_number": "Z-1320-2013",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "64650",
      "termination_date": "20130701",
      "more_code_info": "",
      "recall_initiation_date": "20130130",
      "postal_code": "20878-4000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}