{
  "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": "2026-09-23",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99593",
      "recalling_firm": "embecta Medical II LLC",
      "address_1": "300 Kimball Dr Ste 300",
      "address_2": "N/A",
      "postal_code": "07054-2184",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of MA, KY, CT, TX, NJ, OH, MN, LA, IN, NH, AL, CA, NY, FL, NC, MI, SC, AZ, VA, GA, PA, MO.",
      "recall_number": "Z-3180-2026",
      "product_description": "EWO_02513 (Catalog number 320122)  For Investigational Use Only  Nano Un-Cannulated Demo Samples  Quantity 100",
      "product_quantity": "3000 Final Count (in EA)",
      "reason_for_recall": "Retrospectively reported: Pen needles labeled 'For Investigational Use Only' were inadvertently distributed as commercially marketed devices.",
      "recall_initiation_date": "20230726",
      "center_classification_date": "20260916",
      "report_date": "20260923",
      "code_info": "No UDI/All products labeled \"for Investigational Use Only\"",
      "more_code_info": ""
    }
  ]
}