{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Portage",
      "address_1": "4100 E Milham Ave",
      "reason_for_recall": "The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Manufacturer Part Number 0702-001-000 (120V)  All serial numbers",
      "center_classification_date": "20140131",
      "distribution_pattern": "Nationwide and Canada, Germany, Australia, New Zealand",
      "state": "MI",
      "product_description": "Neptune 2 Rover Ultra Waste Management System.",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "recall_number": "Z-0902-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67191",
      "termination_date": "20160112",
      "more_code_info": "",
      "recall_initiation_date": "20131230",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}