{
  "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": "88327",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "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 Nationwide distribution in the states of FL, MI, NY, TX, WI.",
      "recall_number": "Z-2578-2021",
      "product_description": "PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM  Catalog Number: FC700SU",
      "product_quantity": "80 units",
      "reason_for_recall": "Malfuncton-Implant did not deploy successfully  may necessitate the need for an additional medical intervention for patients which would result in a potential delay in surgery",
      "recall_initiation_date": "20210416",
      "center_classification_date": "20210927",
      "termination_date": "20230118",
      "report_date": "20211006",
      "code_info": "All batch codes"
    }
  ]
}