{
  "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": "Ongoing",
      "city": "Twinsburg",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88367",
      "recalling_firm": "Hitachi Healthcare Americas Corporation",
      "address_1": "1959 Summit Commerce Park",
      "address_2": "N/A",
      "postal_code": "44087-2371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-2308-2021",
      "product_description": "Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation during  robotic/non-robotic intra-operative and laparoscopic procedures",
      "product_quantity": "120 units",
      "reason_for_recall": "The screw cover at the tip of the probe may fall off after a cleaning and sterilization process. Users advised to conduct a preventive   inspection of the probe before and after  sterilization/disinfection/cleaning and  before and after an interoperative procedure.",
      "recall_initiation_date": "20210630",
      "center_classification_date": "20210816",
      "report_date": "20210825",
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