{
  "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": "Libertyville",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96181",
      "recalling_firm": "Hollister Incorporated",
      "address_1": "2000 Hollister Dr",
      "address_2": "N/A",
      "postal_code": "60048-3781",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-1179-2025",
      "product_description": "AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,",
      "product_quantity": "45 box / 540 eaches",
      "reason_for_recall": "Hollister received reports of decreased skin barrier wear time which could can lead to tube migration",
      "recall_initiation_date": "20241223",
      "center_classification_date": "20250219",
      "report_date": "20250226",
      "code_info": "UDI/DI 00610075095834, Lot Numbers:  4L172, 4L182"
    }
  ]
}