{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89123",
      "recalling_firm": "Abbott",
      "address_1": "5050 Nathan Ln N",
      "address_2": "",
      "postal_code": "55442-3209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the state of Missouri and the country of Australia.",
      "recall_number": "Z-0420-2022",
      "product_description": "Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM",
      "product_quantity": "10 units",
      "reason_for_recall": "As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis Introducer devices was  manufactured with an incorrect hub and overall length. The devices manufactured were 12 cm in  length instead of the intended 5 cm in length.",
      "recall_initiation_date": "20211116",
      "center_classification_date": "20211227",
      "termination_date": "20240618",
      "report_date": "20220105",
      "code_info": "Model 407831, Lot 7748246, GTIN: 15414734008805",
      "more_code_info": ""
    }
  ]
}