{
  "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": 1
    }
  },
  "results": [
    {
      "cfres_id": "181768",
      "product_res_number": "Z-2474-2020",
      "event_date_initiated": "2020-06-02",
      "event_date_created": "2020-06-30",
      "recall_status": "Open, Classified",
      "res_event_number": "85782",
      "product_code": "MVR",
      "k_numbers": [
        "K191252"
      ],
      "product_description": "Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only",
      "code_info": "Product Code: 5156-00000-011, All Serial numbers",
      "firm_fei_number": "1417572",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "city": "Deerfield",
      "state": "IL",
      "postal_code": "60015-4625",
      "reason_for_recall": "A firmware issue may cause the GEM1020M-2 Flow Coupler Monitor to intermittently shut down when a WiFi connection is not established.",
      "root_cause_description": "Device Design",
      "action": "Synovis Micro Companies Alliance (MCA), Inc., a subsidiary of Baxter International Inc., sent a notification to healthcare providers dated, June 2, 2020 titled, \"Urgent Medical Device Recall\".  The notification was sent to the user level for the GEM1020M-2 Flow Coupler Monitor due to a firmware issue which may cause the monitor to intermittently shut down when a WiFi connection is not established. If a shutdown occurs, the monitor can be manually powered back on and will resume normal operation. Synovis is requesting the return of the monitors to perform a firmware upgrade to resolve the issue. \n\nCustomers should contact Synovis to arrange for product return for the firmware upgrade and replacement of the product. Customers should complete the Baxter customer reply form and return it to Baxter by scanning and e-mailing it to fca@baxter.com, even if customers do not have any inventory. Customers should return the response form promptly. If customers have distributed the product to other facilities or departments within the institution, a copy of the communication should be forwarded to them.\n\nQuestions regarding the communication, contact Synovis at 800-510-3318 or 205-941-0111, between the hours of 8:00 am and 5:00 pm Central Time, Monday through Friday.",
      "product_quantity": "60 units",
      "distribution_pattern": "U.S. distribution only: VA, GA, MD, PA, DC, WI, LA, MN, FL, IN, MI, AZ, TX, MS, MA, NY, SC, WI, WA, MI, CA.",
      "openfda": {
        "k_number": [
          "K040163",
          "K190499",
          "K093310",
          "K143589",
          "K142309",
          "K132727",
          "K191252",
          "K090679",
          "K861985"
        ],
        "registration_number": [
          "1416980",
          "2183967",
          "1062741",
          "2183744"
        ],
        "fei_number": [
          "2183744",
          "1416980",
          "1000115735",
          "3000302153"
        ],
        "device_name": "Device, Anastomotic, Microvascular",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4300",
        "device_class": "2"
      }
    }
  ]
}