{
  "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": "2026-09-02",
    "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": "99607",
      "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": "Worldwide - US Nationwide distribution in the states of Kansas and Florida. The countries of Australia, European Union, Japan.",
      "recall_number": "Z-3035-2026",
      "product_description": "POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action.    GEI / Electrosurgical, cutting & coagulation & accessories",
      "product_quantity": "335 units",
      "reason_for_recall": "Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.",
      "recall_initiation_date": "20260818",
      "center_classification_date": "20260826",
      "report_date": "20260902",
      "code_info": "Model Number: PS-0523CJDA. UDI-DI: 00821925044531. Lot Number: FR490902."
    }
  ]
}