{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "75571",
      "product_res_number": "Z-0865-2009",
      "event_date_initiated": "2008-08-06",
      "event_date_posted": "2009-01-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-09-11",
      "res_event_number": "50516",
      "product_description": "REF: 915-1000 Lactosorb, Office Fixation Kit, 1 Screwdriver, 1 Tap Handle, 1 Drill Bit, 1 Screw Extractor, 1 Self Drilling Tap, S/S. Aluminum , Teflon, Ra del.   Non Sterile Product.  W.LORENZ SURGICAL, Walter Lorenz Surgical, Inc. 1520 Tradeport Drive Reply to Post Office Box 18009 Jacksonville, Florida 32229-8009 USA 1-800-874-7711. \nAid in the alignment and stabilization of bone in the oral cranio-maxillofacial skeletal system.",
      "code_info": "Lot Numbers: 056960, 060930, 071130, 085650, 155540, 181390, 2247100, 248520, 368120, 584110, 716090, 716100, 716110, 717510, 782200, 851620, 990550, and 999999.",
      "firm_fei_number": "1032347",
      "recalling_firm": "Biomet Microfixation, Inc.",
      "address_1": "1520 Tradeport Dr",
      "city": "Jacksonville",
      "state": "FL",
      "postal_code": "32218-2480",
      "additional_info_contact": "904-741-4400",
      "reason_for_recall": "Biomet Microfixation is recalling the Lactosorb Endobrow Lift Complete, Office Fixation Kit, 1.5/IMF Small Office Set and IMF Set trays containing instruments associated with the Lactosorb and IMF systems.  The finished trays were packaged and shipped to facilities without the instructions for use and without the single use symbol on the packaged tray label.",
      "root_cause_description": "Other",
      "action": "An IFU and correction letter will be issued to the field. Each distributor will receive instructions for delivering the correction letter to all customers. The customer letter will contain a reconciliation form to be returned once the customer receives the IFU for the twist drill.  Contact Biomet Microfixation for additional information at 1-800-874-7711.",
      "product_quantity": "285",
      "distribution_pattern": "Distributed domestically throughout the U.S.  Distributed internationally to Argentina, Australia, Canada, Columbia, Hong Kong, Japan, Mexico, New Zealand, Puerto Rico, Taiwan, Thailand, Denmark, France, Netherlands, Greece, Italy, Norway, Finland, Spain, Czech Republic, and Venezuela.",
      "openfda": {}
    }
  ]
}