{
  "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": "92124",
      "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 distribution to States of: FL, TN, TX.",
      "recall_number": "Z-1605-2023",
      "product_description": "HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004",
      "product_quantity": "240 units",
      "reason_for_recall": "The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package.",
      "recall_initiation_date": "20230303",
      "center_classification_date": "20230518",
      "report_date": "20230524",
      "code_info": "UDI-DI: 00862559000487; Lot Number: 11423949"
    }
  ]
}