{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Cardiff",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89580",
      "recalling_firm": "Huntleigh Healthcare Ltd.",
      "address_1": "35 Portmanmoor Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of OK, CA, GA, MI, VA.",
      "recall_number": "Z-0960-2022",
      "product_description": "HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8",
      "product_quantity": "150 devices",
      "reason_for_recall": "Faceplate may become detached from the probe body.",
      "recall_initiation_date": "20220211",
      "center_classification_date": "20220420",
      "termination_date": "20240612",
      "report_date": "20220427",
      "code_info": "Lot Number:  (10) 7842006001 UDI:  (01) 05051968036537 (10) 784006001 (individual) UDI:  (01) 05051968036544 (10) 784006001 (box)",
      "more_code_info": ""
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}