{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "159400",
      "product_res_number": "Z-0170-2018",
      "event_date_initiated": "2017-10-20",
      "event_date_created": "2017-11-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-10-09",
      "res_event_number": "78392",
      "product_code": "MUU",
      "k_numbers": [
        "K092482"
      ],
      "product_description": "Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000.\n\nUsed for fat transfer and liposuction.",
      "code_info": "Lot 12004",
      "firm_fei_number": "3008719017",
      "recalling_firm": "Shippert Medical Technologies",
      "address_1": "6248 S Troy Cir Ste A 6248 S Troy Cir",
      "address_2": "Ste A",
      "city": "Centennial",
      "state": "CO",
      "postal_code": "80111-6485",
      "reason_for_recall": "Potential breach of sterility of the packaging.",
      "root_cause_description": "Packaging process control",
      "action": "A n Urgent: Medical Device Recall letter, dated October 20, 2017, was mailed to the user, identifying the affected device and describing the reason for the recall.  The letter also provided the risk to health involved and discussed how the user can recognize the failure.  Customers were instructed to remove all affected product from their inventory and quarantine them.  Additionally, the letter should be forwarded to all necessary staff.   Customers are to complete the Recall Response letter within 10 calendar days.  Only the affected products listed should be returned per the instructions provided.  Questions should be directed to Customer Service at 800-888-8663.",
      "product_quantity": "56 units",
      "distribution_pattern": "Worldwide Distribution -- United States, Australia, and Netherlands.",
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        "device_name": "System, Suction, Lipoplasty",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.5040",
        "device_class": "2"
      }
    }
  ]
}