{
  "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": "3773 Corporate Pkwy",
      "reason_for_recall": "possibility of the sterility batch being insufficiently sterilized",
      "address_2": "",
      "product_quantity": "3 unit of Lot 837B",
      "code_info": "Lot # 109C and 837B",
      "center_classification_date": "20190909",
      "distribution_pattern": "US Nationwide distribution in the state of CA.",
      "state": "PA",
      "product_description": "CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM  REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aesculap Implant Systems LLC",
      "recall_number": "Z-2496-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83637",
      "termination_date": "20200512",
      "more_code_info": "",
      "recall_initiation_date": "20190807",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}