{
  "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": {
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      "cfres_id": "116034",
      "product_res_number": "Z-0905-2013",
      "event_date_initiated": "2013-01-11",
      "event_date_posted": "2013-03-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-08-31",
      "res_event_number": "64195",
      "product_code": "DZL",
      "k_numbers": [
        "K010690"
      ],
      "product_description": "Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left), Part Number 487.967.\n\nFor mandibular bone lengthening.",
      "code_info": "Part number 487.967 -  Lot numbers 7883454, 3808876, 7824423, 3800758, 3817116, 3794466",
      "firm_fei_number": "3005180112",
      "recalling_firm": "Synthes USA HQ, Inc.",
      "address_1": "1302 Wrights Ln E",
      "city": "West Chester",
      "state": "PA",
      "postal_code": "19380-3417",
      "additional_info_contact": "customer support\n610-719-5000",
      "reason_for_recall": "It was discovered that the sheer pin on the Multi-Vector Distractor may not be made according to product specifications.",
      "root_cause_description": "Device Design",
      "action": "The firm, Synthes (USA) sent an \"URGENT NOTICE: MEDICAL DEVICE RECALL\" letter dated January 11, 2013 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. Contact the firmat 610-719-5450 for questions regarding this notice.",
      "product_quantity": "18",
      "distribution_pattern": "Nationwide Distribution-including the states of CO, LA, MD, MN, NY, PA, RI, TN, TX and UT.",
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