{
  "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": "2026-06-24",
    "results": {
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      "openfda": {},
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      "recalling_firm": "Orthalign, Inc",
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      "address_2": "",
      "postal_code": "92656-4107",
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      "recall_number": "Z-1630-2026",
      "product_description": "Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7  REF:402567  component Lantern Knee System",
      "product_quantity": "7 units",
      "reason_for_recall": "Drill plates manufactured out of specification can result in a bone cut in excess 00800\"(2.8448mm)",
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      "center_classification_date": "20260324",
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      "code_info": "Lot # 25092204BB/ UDI:00810832032434",
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