{
  "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": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90788",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8229",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide OUS:  AUSTRALIA,  CANADA ,  HONG KONG,  CHINA,  KOREA",
      "recall_number": "Z-1813-2022",
      "product_description": "Olympus POWERSEAL 5MM, 23CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION      Model Number: PS-0523CJDA.  An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.",
      "product_quantity": "27 units (5/box) US; 83 units(5/box) OUS",
      "reason_for_recall": "An out of specification component preventing the blue retention ring from keeping the rotation knob in place. This may result in a loose rotation collar and retention ring and cause delay of treatment",
      "recall_initiation_date": "20220812",
      "center_classification_date": "20220926",
      "report_date": "20221005",
      "code_info": "UDI-DI: 00821925044531 Lot Numbers:  CA191167 CA191168 CA191169 CA191170"
    }
  ]
}