{
  "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": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64285",
      "recalling_firm": "DePuy Orthopaedics, Inc.",
      "address_1": "700 Orthopaedic Dr",
      "address_2": "N/A",
      "postal_code": "46582-3994",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including the states of ME, MA, PA, MD, FL, LA, IL, IA, OH, MN, TX, MT, WA, CA, HI, NV, AZ, KY, WI, CO, GA, MI, TN, NY, AR, NC and VA and the countries of  Canada, Chile, Germany, Czech Republic, Israel , Norway, Poland, Slovenia, Australia, New Zealand, South Africa, Belgium, Austria, Switzerland, France, England and County Cork, Ireland.",
      "recall_number": "Z-0972-2013",
      "product_description": "ReClaim Reamer Extension; Product code 2975-00-500, used with Reclaim Modular Revision Hip Prosthesis System. The ReClaim Reamer Extension is as an attachment to the distal reamers to allow the surgeon to clear soft tissue while reaming the distal femoral canal.",
      "product_quantity": "750",
      "reason_for_recall": "The tabs on the reamer extension device have broken. DePuy is notifying surgeons of the issue to increase the awareness and to ask surgeons and users to look for tabs before and after surgery to reduce any potential that the tabs are left in the patient.  Once the root cause is determined and a design change is implemented, DePuy will conduct a formal swap-out of the affected devices.",
      "recall_initiation_date": "20130225",
      "center_classification_date": "20130320",
      "termination_date": "20131230",
      "report_date": "20130327",
      "code_info": "Engraved Lot Number/  Label Lot Number  J0111 / 578910   578913   R578910   R578912   R578913   In Kit # 2975-50-025  J0211/ In Kit # 2975-50-025  J0411/ 582631   In Kit # 2975-50-025  J0611/ In Kit # 2975-50-025  J0911/ 592125   In Kit # 2975-50-025  J1211/ 000003583   In Kit # 2975-50-025  NB12649 / NB12649  NB12650 / NB12650  NB12651 / NB12651  NB12652 / NB12652  NB12653/ NB12653  NB12654/ NB12654  NB12655/ NB12655  NB12656/ NB12656  NB23480/ NB23480  NB23481/ NB23481  NB3584 / In Kit # 2975-50-025  NB3586 /  NB3586  NB3587 / NB3587  NB3588 / In Kit # 2975-50-025  NB3590 / NB3590  NB3591 / In Kit # 2975-50-025  NB5955 / NB5955  NB7894 / NB7894   In Kit # 2975-50-025  NB8016 / In Kit # 2975-50-025  NB8017 / NB8017  NB8018 / NB8018   In Kit # 2975-50-025  NB8019 / In Kit # 2975-50-025  NB8020 / NB8020  NB8021 / NB8021  NB8022 / NB8022  NB8023 /NB8023"
    }
  ]
}