{
  "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": "2026-07-08",
    "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": "97649",
      "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": "Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada.",
      "recall_number": "Z-0309-2026",
      "product_description": "Brand Name: Aesculap  Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER  Model/Catalog Number: EK083P  Software Version: N/A  Product Description: SEALING UNIT F/10/12MM TROCARS W.REDUCER  Component: N/A",
      "product_quantity": "26 units",
      "reason_for_recall": "It was determined there is the potential of silicone fragments detaching from the yellow sealing component.",
      "recall_initiation_date": "20250924",
      "center_classification_date": "20251024",
      "report_date": "20251105",
      "code_info": "Model No EK083P; UDI-DI: 04046963417710; Lots 52978946, 52991996, 53002275, 53004669, 53006807, 52941286, 52956527, 52956740, 52956952, 52957393, 52967167"
    }
  ]
}