{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Arvada",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89818",
      "recalling_firm": "Sartorius Corporation",
      "address_1": "6542 Fig St",
      "address_2": "",
      "postal_code": "80004-1042",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0946-2022",
      "product_description": "Virus Counter Platform with Model Name VC3100",
      "product_quantity": "82",
      "reason_for_recall": "The Virus Counter is an automated laboratory instrument that enables rapid quantification of intact viruses in solution. This instrument is not a medical device. The virus quantification is used in process development and manufacturing of various biotechnology products such as vaccines, gene therapy and personalized immunotherapy. Device is a Class 1 laser flow cytometer.",
      "recall_initiation_date": "20220311",
      "center_classification_date": "20220415",
      "report_date": "20220427",
      "code_info": "Model Numbers VIR-92166, VIR-92341",
      "more_code_info": ""
    }
  ]
}