{
  "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": "East Taunton",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71470",
      "recalling_firm": "Omnilife Science Inc.",
      "address_1": "50 Oconnell Way Ste 10",
      "address_2": "N/A",
      "postal_code": "02718-1394",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of OK, CO, OH, MA and the countries of Spain and Australia.",
      "recall_number": "Z-2454-2015",
      "product_description": "Offset Femoral Alignment Guide, 2mm x 6¿; Product Code: KS 67022    Product Usage:  The instrumentation has been designed to facilitate bone preparation and implantation of the Apex Knee\u001d or Apex Hip\u001d Systems",
      "product_quantity": "15",
      "reason_for_recall": "The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are incorrect. Specifically, the markings on the alignment guides are reversed from the intended position that should provide proper alignment for the offset revision stems when used with the femur.",
      "recall_initiation_date": "20150609",
      "center_classification_date": "20150824",
      "termination_date": "20150928",
      "report_date": "20150902",
      "code_info": "Lot Numbers: MM0314R, VA0713, Z1111"
    }
  ]
}