{
  "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": "161434",
      "product_res_number": "Z-0803-2018",
      "event_date_initiated": "2017-09-07",
      "event_date_created": "2018-02-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-08-23",
      "res_event_number": "79141",
      "product_code": "JEB",
      "product_description": "The 2nd Assist Knee Positioner",
      "code_info": "Item# 740026",
      "firm_fei_number": "1825034",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "city": "Warsaw",
      "state": "IN",
      "postal_code": "46582-6989",
      "additional_info_contact": "411 Technical Services\n574-371-3071",
      "reason_for_recall": "Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.",
      "root_cause_description": "Package design/selection",
      "action": "On September 12, 2017 an URGENT MEDICAL DEVICE RECALL notice was issued to distributors and customers titled \"The Second Assistant Disposable Knee Positioner\". The notice requests customers to review their inventory and to quarantine any remaining product, which will be returned to the firm. Also, to notify any additional accounts which may have received product from you. Questions or concerns can be directed to Customer Service at 574-371-3071",
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      "distribution_pattern": "Nationally",
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        "device_name": "Table, Surgical With Orthopedic Accessories, Manual",
        "medical_specialty_description": "General, Plastic Surgery",
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