{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Stillwater",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86152",
      "recalling_firm": "Diasorin Inc.",
      "address_1": "1951 Northwestern Ave S",
      "address_2": "N/A",
      "postal_code": "55082-7536",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "NJ, WI, NY, NC, MN, CA, IL, VA, MA, MI, CT    Canada",
      "recall_number": "Z-2936-2020",
      "product_description": "Parvovirus B19 IgG EIA kit   Part No. V519IGUS",
      "product_quantity": "615 units",
      "reason_for_recall": "Printed label inside the box  lid of the Parvovirus has the incorrect Lot Specific Constant value",
      "recall_initiation_date": "20200717",
      "center_classification_date": "20200903",
      "report_date": "20200909",
      "code_info": "Lot 71440040AA"
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}