{
  "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": "Powell",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93520",
      "recalling_firm": "DeRoyal Industries Inc",
      "address_1": "200 Debusk Ln",
      "address_2": "",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US:  Virginia",
      "recall_number": "Z-0622-2024",
      "product_description": "DeRoyal CARDIAC CATH SET-UP KIT PGYBK, REF 89-10572",
      "product_quantity": "252 units",
      "reason_for_recall": "Kit were manufactured and distributed with Edwards Life Sciences TruWave Disposable pressure transducers which were subsequently recalled by Edwards Life Sciences.",
      "recall_initiation_date": "20231122",
      "center_classification_date": "20231228",
      "report_date": "20240103",
      "code_info": "GTIN 00749756364065, Serial Numbers:  '59716839, '59867186",
      "more_code_info": ""
    }
  ]
}