{
  "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 4503223, Lot #142345647, 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 (24) (Catalog number 4503223)     Product Usage:  The artus CMV RG PCR ASR  is designed to detect and to quantify nucleic acid specific to human cytomegalovirus (CMV) using real-time  PCR technology (PCR) in the Rotor-Gene 2000/3000 (RG).",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "QIAGEN Gaithersburg, Inc.",
      "recall_number": "Z-1321-2013",
      "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"
    }
  ]
}