{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "700 Orthopaedic Dr",
      "reason_for_recall": "Specific lots are being recalled due to the potential for the tabs to break, leaving fragments in the patient.",
      "address_2": "",
      "product_quantity": "875 units",
      "code_info": "J0111,  J0211,  J0411,  J0611,  J0911,  J1211,  NB12649,  NB12650,  NB12651,  NB12652,  NB12653,  NB12654,  NB12655,  NB12656,  NB23480,  NB23481,  NB3584,  NB3586,  NB3587,  NB3588,  NB3590,  NB3591,  NB5955,  NB7894,  NB8016,  NB8017,  NB8018,  NB8019,  NB8020,  NB8021,  NB8022,  NB8023,  578910,  578913,  R578910,  R578912,  R578913,  582631, and   592125.",
      "center_classification_date": "20141007",
      "distribution_pattern": "Worldwide Distribution -- USA, including the states of ME, MD, PA, MA, FL, LA, IL, IA, OH, MN, TX, MT, WA, CA, HI, NV, AZ, KY, WI, CO, GA, MI, NC, VA, NY, TN, and IN; and, the countries of Canada, Australia, Austria, Belgium, Czech Republic, United Kingdom, France, Germany, Ireland, Israel, New Zealand, Norway, Poland, Slovenia, South Africa, Switzerland, and Chile.",
      "state": "IN",
      "product_description": "RECLAIM Distal Reamer Extension   Non Sterile  REF 2975-00-500    Intended as an attachment device to the distal reamers to allow the surgeon to clear soft tissue while reaming the distal femoral canal.",
      "report_date": "20141015",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "recall_number": "Z-0038-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "69104",
      "termination_date": "20151109",
      "more_code_info": "",
      "recall_initiation_date": "20140903",
      "postal_code": "46582-3994",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}