{
  "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": "91840",
      "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": "US Nationwide Distribution",
      "recall_number": "Z-1418-2023",
      "product_description": "Single Use Rotatable Clip Fixing Device    Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip  Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip  Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip",
      "product_quantity": "65.9 boxes (373 pieces)",
      "reason_for_recall": "There have been complaints that the clip did not come out of the tube sheath during the procedure.",
      "recall_initiation_date": "20230223",
      "center_classification_date": "20230420",
      "report_date": "20230426",
      "code_info": "1) UDI-DI 14953170353106; Model HX-201LR-135; Lot 1ZV  2) UDI-DI 14953170353113; Model HX-201UR-135; Lot 23V  3) UDI-DI 14953170353120; Model HX-201UR-135; Lot 24V  4) UDI-DI 14953170353168; Model HX-201UR-135L; Lot 24V"
    }
  ]
}