{
  "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": "Stafford Springs",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90769",
      "recalling_firm": "Hobbs Medical, Inc.",
      "address_1": "8 Spring St",
      "address_2": "N/A",
      "postal_code": "06076-1505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.",
      "recall_number": "Z-0011-2023",
      "product_description": "Hobbs Medical Spray Catheter: The Mistifier: \t2.6mm\t165cm   Disposable For endoscopy procedures  Ref: 2191",
      "product_quantity": "30 units",
      "reason_for_recall": "Device label display an incorrect expiration date, extends the shelf life of the product. Affected product  distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)",
      "recall_initiation_date": "20220729",
      "center_classification_date": "20221007",
      "report_date": "20221019",
      "code_info": "UDI-DI: M84921910 Lot Numbers: H03-16-015R"
    }
  ]
}