{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Guilford",
      "state": "ME",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94087",
      "recalling_firm": "Puritan Medical Products Company, Llc",
      "address_1": "31 School St",
      "address_2": "N/A",
      "postal_code": "04443-6388",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AL, CA, FL, GA, IA, ID, IL, IN, KY, MA, MI, MO, NC, NJ, NY, OH, OK, PA, TX, VA and the countries of Canada, P.R. China and Thailand.",
      "recall_number": "Z-1391-2024",
      "product_description": "HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.",
      "product_quantity": "465 boxes x 500 units per box = 232,500 units",
      "reason_for_recall": "It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in all packages.",
      "recall_initiation_date": "20240221",
      "center_classification_date": "20240328",
      "report_date": "20240403",
      "code_info": "Part number: 25-3317-H; UDI/DI: 00609576330322; Serial/Lot Number: S1014;",
      "more_code_info": ""
    }
  ]
}