{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91533",
      "recalling_firm": "Access Vascular, Inc",
      "address_1": "749 Middlesex Tpke",
      "address_2": "N/A",
      "postal_code": "01821-3906",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CT, FL, NE, TN, TX, WA.",
      "recall_number": "Z-1156-2023",
      "product_description": "HydroMID 4Fr Single Lumen   Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy  Product Number: 80004004",
      "product_quantity": "445 units",
      "reason_for_recall": "Label with the incorrect component listed on the inner kit Tyvek header bag",
      "recall_initiation_date": "20221222",
      "center_classification_date": "20230222",
      "report_date": "20230301",
      "code_info": "UDI-DI: (01)00850030354020 Lot Numbers: 11424032, 11432076"
    }
  ]
}