{
  "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": "East Taunton",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62912",
      "recalling_firm": "Omni Life Science",
      "address_1": "50 Oconnell Way",
      "address_2": "Unit 10",
      "postal_code": "02718",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide including the states of CO, NY, OK, PA, UT, VA, and WI, and the countries of Spain and the Netherlands.",
      "recall_number": "Z-2375-2012",
      "product_description": "Omnilife Science Apex Knee System Modular Tibia Augment, Size 6 x 4mm  Ref: KC-54060.    The Apex Knee System is intended for use as a primary or revision total knee replacement.",
      "product_quantity": "36 units",
      "reason_for_recall": "The Apex Knee System Modular Tibia Augment may breach the inner and outer sterile pouches, compromising the sterility",
      "recall_initiation_date": "20120809",
      "center_classification_date": "20120913",
      "termination_date": "20130110",
      "report_date": "20120919",
      "code_info": "Lot Numbers: 10723, 10763, 10824"
    }
  ]
}