{
  "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": "Raynham",
      "address_1": "325 Paramount Dr",
      "reason_for_recall": "Specific units of the DePuy Mitek Sterile Reamers are not labeled correctly,  7 units were labeled as 11MM while the box actually contained a 10 MM reamer",
      "address_2": "",
      "product_quantity": "20",
      "code_info": "Lot Number: 3611687",
      "center_classification_date": "20121217",
      "distribution_pattern": "Nationwide Distribution including IL and NJ",
      "state": "MA",
      "product_description": "DePuy Mitek 11 MM Fully Fluted Reamer, Sterile  Product Number: 232423    DePuy Mitek Sterile Reamers are intended to cut through cortical and cancellous bone during Cruciate Ligament Repair/Reconstruction of the knee.",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DePuy Mitek, Inc., a Johnson & Johnson Co.",
      "recall_number": "Z-0529-2013",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "63732",
      "termination_date": "20121221",
      "more_code_info": "",
      "recall_initiation_date": "20121116",
      "postal_code": "02767",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}