{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "190573",
      "product_res_number": "Z-0403-2022",
      "event_date_initiated": "2021-12-01",
      "event_date_created": "2021-12-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2024-02-28",
      "res_event_number": "89119",
      "product_code": "MAL",
      "k_numbers": [
        "K954848"
      ],
      "product_description": "Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890",
      "code_info": "Lot number: 20C04;\n\nSerial Numbers: 1260004700 and 1259882880;\n\nUDI Code:\n(01)00384401017752(11)200304(17)250228(21)1260004700GS(10)20C04\n(01)00384401017752(11)200304(17)250228(21)1259882880GS(10)20C04",
      "firm_fei_number": "2242352",
      "recalling_firm": "Maquet Cardiovascular, LLC",
      "address_1": "45 Barbour Pond Dr",
      "city": "Wayne",
      "state": "NJ",
      "postal_code": "07470-2094",
      "reason_for_recall": "There is a probable mislabeling of product.  A Hemashield Platinum Woven Double Velour Bifurcated Vasuclar Graft, SN 1259735369, 24 mm x 12 mm, REF Number M00202166241P0 is likely packaged inside of the carton instead of a Hemashield Gold Knitted Microvel Double Velour Bifurcated Vascular Graft; SN 1260004700; 18 mm x 9 mm; REF Number M002020851890 or a Hemashield Gold Knitted Microvel Double Velour Bifurcated Vascular Graft; SN 1259882880; 18 mm x 9 mm; Ref Number M002020851890.",
      "root_cause_description": "Labeling Change Control",
      "action": "And URGENT MEDICAL DEVICE REMOVAL notification letter dated 12/1/21 was sent to customers.\n\nActions to be taken:\n\" If you have already implanted one of the above-mentioned devices, kindly notify us as soon as possible by contacting your Getinge representative or Customer Service (at 1-888-943-8872, options 2), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. EST. You will be contacted shortly by our Medical Affairs Officer in order to discuss the appropriate follow up.\n\" Please examine your inventory immediately to determine if you one of the Hemashield Gold Knitted Bifurcated Vascular Graft with a Serial Number matching those listed on page 1 of this letter.\n\" Should you have un-used affected product, you are eligible for credit or a replacement at no cost to your facility upon receipt of Response Form (see page 4).\n\" To get your free replacement Graft we need you to provide a ship to contact and your\nacknowledgment on page 4.\n\" Please contact Getinge Customer Service at 1-888-943-8872, (press option 2) Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone), to request shipping instructions to return any affected product.\n\" Pack the product to be returned with the appropriate return documents.\n\" Whether you have affected product or not, please complete and sign the attached URGENT\nMEDICAL DEVICE REMOVAL   RESPONSE FORM (page 4) to acknowledge this recall and return the completed form to Getinge by e-mailing a scanned copy to\nHemashield.Intervascular@getinge.com or by FAX to 877-258-1332.\n\" Please forward this information to all current and potential Hemashield Gold Knitted Microvel double velour vascular graft users within your hopsital / facility.\n\" If you are a distrubutor who has shipped any affected product to customers, please forward this document to their attention for appropriate action.\nThis voluntary recall only affects the product with the serial number and lot number listed on page 1; no other products",
      "product_quantity": "2",
      "distribution_pattern": "US Nationwide distribution in the states of IL and NC.",
      "openfda": {
        "k_number": [
          "K052302",
          "K103080",
          "K122612",
          "K021213",
          "K954848",
          "K093231"
        ],
        "pma_number": [
          "P890045",
          "P920027"
        ],
        "registration_number": [
          "",
          "3010162973",
          "9612515",
          "3010407203",
          "1220948",
          "1640201",
          "2246552"
        ],
        "fei_number": [
          "3002707083",
          "",
          "3010407203",
          "3002808437",
          "1220948",
          "2246552",
          "3002807041"
        ],
        "device_name": "Graft, Vascular, Synthetic/Biologic Composite",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.3450",
        "device_class": "2"
      }
    }
  ]
}