{
  "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": "2026-04-29",
    "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": "69600",
      "recalling_firm": "Aesculap, Inc.",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution in Kansas only.",
      "recall_number": "Z-0502-2015",
      "product_description": "The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.",
      "product_quantity": "1",
      "reason_for_recall": "Aesculap Inc. (AIC (USA)) initiated a recall of Miethke Shunt System, Dual Switch Valve, due to incorrect product labeling on three units.  The incorrect product labeling was the wrong expiration date, 2024-09, on the inner labeling of the sterile bag.  However, the expiration date on the outer box was correct.  No patient injuries were reported as a result of this issue.",
      "recall_initiation_date": "20141024",
      "center_classification_date": "20141203",
      "termination_date": "20150520",
      "report_date": "20141210",
      "code_info": "Item Number FV129  Lot Number 4506244166  Serial Number A10150"
    }
  ]
}