{
  "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": "2026-09-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "217912",
      "product_res_number": "Z-1218-2026",
      "event_date_initiated": "2025-12-05",
      "event_date_posted": "2026-01-29",
      "recall_status": "Open, Classified",
      "res_event_number": "98218",
      "product_code": "MGZ",
      "k_numbers": [
        "K221902"
      ],
      "product_description": "Brand Name: LimFlow Vector\nProduct Name: LimFlow Vector\nModel/Catalog Number: VT-US-23",
      "code_info": "Lot Code: Model: VT-US-23\nLot: 82321838\nGTIN: 00850041730134\nU.S. Product Code: MGZ",
      "firm_fei_number": "3023527320",
      "recalling_firm": "LimFlow, Inc.",
      "address_1": "3031 Tisch Way Ste 110 3031 Tisch Way",
      "address_2": "Ste 110",
      "city": "San Jose",
      "state": "CA",
      "postal_code": "95128-2541",
      "reason_for_recall": "Incorrect expiration date",
      "root_cause_description": "Process control",
      "action": "On December 11, 2025, Stryker ( LimFlow Inc.) issued a Urgent Medical Device Recall Notification letter. Stryker ask consignees to take the following actions:\n\n1. Immediately check your internal inventory to locate the product(s) listed on the attached Business Reply Form, remove them from their point of use, and isolate/quarantine the unit(s) to prevent accidental use.\n\n2. Sign and return the enclosed Business Reply Form by email to  to confirm receipt of this notification/documenting product segregation.\n\n3. Upon receipt of the completed Business Reply Form, Stryker will contact you to arrange for the return and replacement of your product(s).\n\n4. Maintain awareness of this communication internally until all required actions have been completed within your facility.\n\n5. If you have further distributed the affected product, please notify the applicable parties at once about this recall. You may copy and distribute this notification letter.",
      "product_quantity": "33 units",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CT, District of Columbia, FL, KY, MA, MI, NE, NJ, NY, OH, PA, RI, TX, WY.",
      "openfda": {
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          "K980723",
          "K912635",
          "K080178",
          "K946352",
          "K250105",
          "K912636",
          "K914385",
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          "K925283",
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          "K965137",
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          "K022823",
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          "K924171",
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          "K140042",
          "K260188",
          "K932009",
          "K111884",
          "K142660",
          "K221902"
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        "registration_number": [
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          "3027735872",
          "3009039068",
          "3003637635",
          "3011137372",
          "1319639",
          "1220948",
          "8010697",
          "3010041511",
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          "3009018440",
          "2126670",
          "3045042524"
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        "fei_number": [
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          "3027735872",
          "3009039068",
          "3003637635",
          "1000138054",
          "1220948",
          "3010041511",
          "3023527320",
          "3009018440",
          "2126670",
          "3005747797",
          "3004053982",
          "3045042524"
        ],
        "device_name": "Valvulotome",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.4885",
        "device_class": "2"
      }
    }
  ]
}