{
  "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": "2026-09-08",
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      "manufacturer_g1_country": "US",
      "manufacturer_contact_city": "MAHWAH",
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      "mdr_text": [
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          "mdr_text_key": "393902129",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "THE FOLLOWING WAS REPORTED: SURGEON COMPLAINED POST-OP ABOUT CUP PLACEMENT AND IT NOT BEING IN HIS 45/20 ANGLE. REVISION SURGERY PERFORMED SAME DAY TO ONLY RE-POSITION THE CUP. CASE TYPE / APPLICATION: THA 4.1."
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      "suppl_dates_fda_received": "06/16/2026"
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}