{
  "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": "90232",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "",
      "postal_code": "18034-8229",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AL, FL, NC, NY.",
      "recall_number": "Z-1275-2022",
      "product_description": "EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum).  Model: GIF-HQ190",
      "product_quantity": "8 units",
      "reason_for_recall": "Part (A-rubber) intended for a different model of gastrointestinal videoscope may have been used when  replacing part on GIF-HQ190 during the last repair at  Olympus. An Incorrect A-rubber fits tighter on the GIF-HQ190 which would not meet the intended design specifications",
      "recall_initiation_date": "20220422",
      "center_classification_date": "20220621",
      "report_date": "20220629",
      "code_info": "UDI-DI: 04953170305276 Serial: 2269931, 2611873, 2613235, 2634251, 2634326, 2860721, 2961773 and 2962545",
      "more_code_info": ""
    }
  ]
}