{
  "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": {
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      "status": "Terminated",
      "city": "Saint Cloud",
      "state": "MN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90761",
      "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",
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      "recall_number": "Z-1740-2022",
      "product_description": "Helix Elite Inactivated Standard, labeled as:     a. Inactivated SARS-CoV-2 B.1.1.7 Whole Virus, REF HE0071N;   b. Inactivated SARS-CoV-2 B.1.351 Whole Virus, REF HE0073N",
      "product_quantity": "2",
      "reason_for_recall": "Product not registered for use in the UK",
      "recall_initiation_date": "20220727",
      "center_classification_date": "20220916",
      "termination_date": "20240802",
      "report_date": "20220921",
      "code_info": "a. UDI Number: 10845357043846, Lot Number: HE0071-01-1, Expiration Date: 12/31/2022. b. UDI Number: 10845357043945, Lot Number: HE0073-02-2, Expiration Date: 02/28/2023.",
      "more_code_info": ""
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}