{
  "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": {
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      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90537",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
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      "distribution_pattern": "United States: CO",
      "recall_number": "Z-1406-2022",
      "product_description": "LEFT CORONAL BENDER, TEK1939. Instrument used during spinal surgery.",
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      "reason_for_recall": "Customized coronal rod benders may deform the implant when used with the spinal system devices.",
      "recall_initiation_date": "20210630",
      "center_classification_date": "20220719",
      "termination_date": "20240417",
      "report_date": "20220727",
      "code_info": "LOT: 2930901A"
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