{
  "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": "91426",
      "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, IL, IN, MA, NE, TN, and TX.",
      "recall_number": "Z-1129-2023",
      "product_description": "HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002",
      "product_quantity": "1,789 HydroMID devices",
      "reason_for_recall": "Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.",
      "recall_initiation_date": "20221216",
      "center_classification_date": "20230210",
      "report_date": "20230222",
      "code_info": "UDI-DI: (01)00850030354006; Lot Number: 11428361, 11393260, 11395226"
    }
  ]
}