{
  "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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      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89903",
      "recalling_firm": "Conformis, Inc.",
      "address_1": "600 Technology Park Dr Ste 3",
      "address_2": "N/A",
      "postal_code": "01821-4154",
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      "reason_for_recall": "Incorrect tibial base plate implant packaged in kit",
      "recall_initiation_date": "20220222",
      "center_classification_date": "20220408",
      "report_date": "20220420",
      "code_info": "Serial Number: 0496242  UDI: M572TPS3011113011"
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}