{
  "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": "2026-04-15",
    "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": "70692",
      "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: US (nationwide) in CA;  Ireland and Israel.",
      "recall_number": "Z-1357-2015",
      "product_description": "RECLAIM Assembled Implant Inserter Adaptor  orthopedic manual surgical instrument for hip implantation.",
      "product_quantity": "54 of Lot No: SO2018074",
      "reason_for_recall": "This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may fracture during surgery and there is the potential for plastic pieces to be left in the patient.",
      "recall_initiation_date": "20150223",
      "center_classification_date": "20150331",
      "termination_date": "20150928",
      "report_date": "20150408",
      "code_info": "CATALOG NO. : 2975-00-920:   Barcode (GTIN): 10603295156192  Lot No.  Distribution  SO2018074 (Distributed)  SO2018072 (Not Distributed)  SO2018073 (Not Distributed)  SO2018075 (Not Distributed)  SO2018080 (Not Distributed)"
    }
  ]
}