{
  "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": {
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      "city": "Jericho",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95459",
      "recalling_firm": "ImaCor Inc.",
      "address_1": "50 Jericho Tpke Ste 105",
      "address_2": "N/A",
      "postal_code": "11753-1014",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL ,GA,  NJ, TN",
      "recall_number": "Z-0231-2025",
      "product_description": "ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms.  Model/Catalog Number: CLT-010, CLT-010-1",
      "product_quantity": "73 units",
      "reason_for_recall": "Epoxy used to seal the edge of the transducer into its paddle exceeded specification. This variability could attenuate the ultrasound signal with a potential impact on the quality of images obtained from the probes.",
      "recall_initiation_date": "20240916",
      "center_classification_date": "20241025",
      "report_date": "20241106",
      "code_info": "UDI - Primary - 00861589000108 Lot numbers: 20250509 and 20250823",
      "more_code_info": ""
    }
  ]
}