{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 7
    }
  },
  "results": [
    {
      "cfres_id": "170058",
      "product_res_number": "Z-1330-2019",
      "event_date_initiated": "2018-02-02",
      "event_date_created": "2019-05-15",
      "recall_status": "Completed",
      "res_event_number": "81837",
      "product_code": "MUU",
      "k_numbers": [
        "K092482"
      ],
      "product_description": "Tissu-Trans FILTRON 100, Catalog 3-TT-FILTRON 100, sterile, disposable, one-patient use.  The firm name on the label is Shippert Medical Technologies, Centennial, CO.",
      "code_info": "Lot numbers 61472, 61601, 61816, 61817, 61818, 61819, 61878, 61736, 61801, 61948, 62050, and 62139.",
      "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",
      "additional_info_contact": "Customer Service\n651-789-3939",
      "reason_for_recall": "The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.",
      "root_cause_description": "Packaging process control",
      "action": "Letters dated 1/9/2018 were issued beginning 2/2/2018 via registered mail and Fed Ex explaining the reason for recall, risk to health, description of how to recognize the device failed, and actions to be taken.",
      "product_quantity": "6,553 units were distributed for all catalog numbers",
      "distribution_pattern": "Distribution was nationwide, including PR.   There was government/military distribution.\n\nForeign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,",
      "openfda": {
        "k_number": [
          "K171135",
          "K150156",
          "K161372",
          "K092482",
          "K132815",
          "K121005",
          "K142682",
          "K101713",
          "K191564",
          "K163647",
          "K161636",
          "K193539",
          "K190386",
          "K162932",
          "K092284",
          "K100114",
          "K102117",
          "K172714",
          "K120328",
          "K141591",
          "K172717",
          "K190278",
          "K121703",
          "K120902",
          "K182732",
          "K113255",
          "K170449",
          "K081848",
          "K072587",
          "K150779",
          "K083455",
          "K142073",
          "K203800",
          "K210528",
          "K141713",
          "K171242",
          "K202443",
          "K130152",
          "K193363",
          "K092923"
        ],
        "registration_number": [
          "2030624",
          "2953359",
          "2020601",
          "3016080683",
          "3008624479",
          "3011710821",
          "3008717566",
          "2024024",
          "3012441529",
          "3010173425",
          "3021284635",
          "1720734",
          "1066491",
          "3004167969",
          "3017791237",
          "1649660",
          "1420032",
          "2032809",
          "1423662",
          "3010531069",
          "3008719017",
          "1649518",
          "3009420598",
          "1937141",
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          "2030598",
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          "3011707889",
          "3006798004",
          "1220477",
          "1222928",
          "3006053983",
          "2219920",
          "1313525",
          "3010742783",
          "3009882464",
          "1058584",
          "1222993",
          "1211566",
          "3011423170",
          "1054811"
        ],
        "fei_number": [
          "1000114185",
          "3000206435",
          "2020601",
          "3002807036",
          "3016080683",
          "3004169154",
          "1000117446",
          "1000120578",
          "3008624479",
          "3011710821",
          "3008717566",
          "2024024",
          "3012441529",
          "1317628",
          "1000219637",
          "3021284635",
          "1720734",
          "3004106598",
          "3004167969",
          "1000518731",
          "3017791237",
          "3003429569",
          "1420032",
          "3000215273",
          "3010531069",
          "3008719017",
          "3009420598",
          "3007137651",
          "3016467822",
          "3011707889",
          "3006798004",
          "1220477",
          "3006053983",
          "3001236277",
          "2219920",
          "3010742783",
          "3009882464",
          "1000120613",
          "1211566",
          "3001451796",
          "3000215205"
        ],
        "device_name": "System, Suction, Lipoplasty",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.5040",
        "device_class": "2"
      }
    }
  ]
}