{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89446",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "address_2": "",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.",
      "recall_number": "Z-0701-2022",
      "product_description": "Helix Elite\" Molecular Standards: Inactivated Standard.  Inactivated Influenza A/B and Respiratory Syncytial Virus",
      "product_quantity": "1 unit",
      "reason_for_recall": "Real-time shelf life testing failed at 24 months",
      "recall_initiation_date": "20170606",
      "center_classification_date": "20220301",
      "termination_date": "20230117",
      "report_date": "20220309",
      "code_info": "Catalog Number: HE0044N;  Lot Number: HE0044N-103-1;   UDI: 10845357042184",
      "more_code_info": ""
    }
  ]
}