{
  "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": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79268",
      "recalling_firm": "OMNIlife science Inc.",
      "address_1": "480 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the country Spain.",
      "recall_number": "Z-1117-2018",
      "product_description": "Apex Knee System, Tibial Baseplate Size 6 Left, non-porous - KC-2206L    The Apex Knee System is intended for use as a primary or revision total knee replacement. This knee replacement system is intended for cemented fixation and single use implantation. This prosthesis may be used for the following conditions, as appropriate:   Non-inflammatory degenerative joint disease, including osteoarthritis and avascular necrosis;   Rheumatoid arthritis;   Correction of functional deformity;   Revision procedures where other treatments or devices have failed.",
      "product_quantity": "32",
      "reason_for_recall": "The Apex Knee System Tibial Baseplate identified has an improper expiration date marked on the external packaging. The improper expiration date (2202-03) is  marked on the external packaging only. The correct lot number (2022-03) is present in the internal packaging and sterile batch documentation.",
      "recall_initiation_date": "20171120",
      "center_classification_date": "20180319",
      "termination_date": "20190607",
      "report_date": "20180328",
      "code_info": "Product Code KC-2206L, Lot # 26519"
    }
  ]
}