{
  "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": "2026-08-05",
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      "date_added": "20080430",
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      "mdr_report_key": "1001415",
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      "number_devices_in_event": "",
      "date_manufacturer_received": "20080121",
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      "report_source_code": "Manufacturer report",
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      "mdr_text": [
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          "mdr_text_key": "801463",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "IT WAS REPORTED THAT THE 2.4MM PIN (AR-1250L) IN THE DISPOSABLE KIT BROKE DURING AN ANTERIOR CRUCIATE LIGAMENT (ACL) REPAIR. THE PIECE WAS NOT RETRIEVED FROM THE PT. THE CUSTOMER REPORTED NO FURTHER CONSEQUENCES AS A RESULT OF THIS EVENT. NO FURTHER PT INFO IS AVAILABLE FROM THE CUSTOMER. THIS DEVICE IS USED FOR TREATMENT."
        },
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          "text": "THE DEVICE HAS BEEN RECEIVED AND AN EVALUATION IS IN PROGRESS. A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION."
        }
      ],
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}