{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ashland",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89792",
      "recalling_firm": "Terumo Cardiovascular Systems Corp",
      "address_1": "28 Howe St",
      "address_2": "",
      "postal_code": "01721-1305",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US  Nationwide distribution in the states of CA and IN.",
      "recall_number": "Z-0949-2022",
      "product_description": "Cardiovascular Procedure Kit catalog # 76645 & 73806",
      "product_quantity": "64",
      "reason_for_recall": "Potential for Cardiovascular Procedure Kit packaging damage that occurred during shipping.",
      "recall_initiation_date": "20220203",
      "center_classification_date": "20220418",
      "termination_date": "20240220",
      "report_date": "20220427",
      "code_info": "[Lot #Z15957677, case label GTIN: (01)00699753507685, product identifier: (17)230228(10)Z15957677] and [Lot #Z16958398, case label GTIN: (01)00699753477728, product identifier: (17)230228(10)Z16958398]",
      "more_code_info": ""
    }
  ]
}