{
  "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": "Merrimack",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91043",
      "recalling_firm": "Atrium Medical Corporation",
      "address_1": "40 Continental Blvd",
      "address_2": "N/A",
      "postal_code": "03054-4332",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of VA.",
      "recall_number": "Z-0235-2023",
      "product_description": "Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000",
      "product_quantity": "24 units (4cases/6)",
      "reason_for_recall": "Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.",
      "recall_initiation_date": "20221018",
      "center_classification_date": "20221115",
      "report_date": "20221123",
      "code_info": "UDI-DI: 20650862100017 - case / 00650862100013- each Lot Number: 472326, 473226"
    }
  ]
}