{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "74831",
      "product_res_number": "Z-0415-2009",
      "event_date_initiated": "2008-10-24",
      "event_date_posted": "2008-11-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-09-11",
      "res_event_number": "50149",
      "product_code": "FDG",
      "product_description": "Fredrick's Converse Retractor #5 F/O, Model Number: 01-0485.\n\nA fiber optic retractor used in plastic surgery procedures to retract tissue.",
      "code_info": "Lot # 042408D08",
      "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": "Fiber optic cable is missing from the Frederick's Converse Retractor Lot # 042408D08.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Consignee was notified by certified mail via an Urgent Medical Device Recall Notice dated 10/24/08, with return receipt.  The letter identifies the product and states the issue with the product.  The letter required the customer to discontinue use of the item and return it to Biomet Microfixation so that they may rework the instrument.  It also asked the customer to notify any hospital personnel responsible for receiving recall notices of this action if the product had been further distributed.  The RGA number should be utilized to return the products.  The Inventory Reconciliation sheet should be filled out and faxed to 904-741-9425.",
      "product_quantity": "3",
      "distribution_pattern": "Nationwide Distribution --- including states of Chicago, IL and La Crosse, WI.",
      "openfda": {
        "device_name": "Retractor, Fiberoptic",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4530",
        "device_class": "1",
        "k_number": [
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