{
  "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": "2026-03-18",
    "results": {
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  "results": [
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      "status": "Ongoing",
      "city": "Bridgewater",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92627",
      "recalling_firm": "Hamamatsu Corporation",
      "address_1": "360 Foothill Rd",
      "address_2": "N/A",
      "postal_code": "08807-2920",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "NY",
      "recall_number": "Z-2280-2023",
      "product_description": "NanoZoomer S360MD Slide scanner system-automated system for creating, viewing, and managing digital slides. The NanoZoomer System creates diagnostic-quality digital images of glass slides containing formalin-fixed paraffin-embedded (FFPE) tissue.  Catalog Number: C13220-01MD",
      "product_quantity": "1 unit",
      "reason_for_recall": "If the wrong barcode information is recorded in the NDPi file, a pathologist may refer to the whole slide image (WSI) of a different patient.",
      "recall_initiation_date": "20230606",
      "center_classification_date": "20230731",
      "report_date": "20230809",
      "code_info": "UDI-DI: 010458238901065911220 S/N: 90121100033"
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}