{
  "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-0312-2026",
      "product_description": "Brand Name: AESCULAP  Product Name: REDUCING CONVERTER 10/12MM TO 5MM  Model/Catalog Number: EK087P  Software Version: N/A  Product Description: REDUCING CONVERTER 10/12MM TO 5MM  Component: N/A",
      "product_quantity": "155 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 EK087P;  UDI-DI: 04046963620059; Lots 52974276, 52952133, 52954633, 52959357, 52964442, 52968887, 52972214, 52977427, 52981208, 52985519, 52988828, 52992514, 52993617, 52997919, 53002094, 53004347, 53006380, 53007625, 53010869, 53013557"
    }
  ]
}