{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88448",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "PO Box 610",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, GA, MN, TN.",
      "recall_number": "Z-2380-2021",
      "product_description": "Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation, mechanical grasping, and dissection of tissue during the performance of laparoscopic and general open surgical procedures when used in conjunction with the Gyrus ACMI G400 workstation  Ref: 970010PC",
      "product_quantity": "6 boxes (5 per/box)=30 units",
      "reason_for_recall": "Expired adhesive used as an electrical insulation barrier and as a secondary retention bond failed  and could result in foreign body / biologic reaction within the patient and / or electrical continuity to patient causing tissue burn to critical structures.",
      "recall_initiation_date": "20210609",
      "center_classification_date": "20210827",
      "termination_date": "20230217",
      "report_date": "20210908",
      "code_info": "Lot number KR121617"
    }
  ]
}