{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Toano",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98298",
      "recalling_firm": "AVID Medical, Inc.",
      "address_1": "9000 Westmont Dr",
      "address_2": "N/A",
      "postal_code": "23168-9351",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of New Jersey.",
      "recall_number": "Z-1338-2026",
      "product_description": "Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.",
      "product_quantity": "1,500 units",
      "reason_for_recall": "Tyvek bag seal issue which may compromise sterility of the kit.",
      "recall_initiation_date": "20260102",
      "center_classification_date": "20260209",
      "report_date": "20260218",
      "code_info": "Kit Code: LIFE0080-01. UDI-DI: 10809160314500. Lot Number: 1650056. Expiration Date: 07/24/2028"
    }
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}