{
  "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": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3500 Corporate Pkwy",
      "reason_for_recall": "There is a potential for the single use suction valve to come apart and/or remain stuck inside the endoscope.",
      "address_2": "PO Box 610",
      "product_quantity": "310000",
      "code_info": "Lot numbers: 88H, 89H, 8XH, 8YH, 8ZH, 91H",
      "center_classification_date": "20190802",
      "distribution_pattern": "The products were distributed US Nationwide.",
      "state": "PA",
      "product_description": "Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209    Product Usage:  This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible endoscopes include Olympus bronchoscopes, cystoscopes, rhino-laryngoscopes and pleurascopes models.",
      "report_date": "20190814",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus Corporation of the Americas",
      "recall_number": "Z-2148-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82519",
      "termination_date": "20200609",
      "recall_initiation_date": "20190401",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}