{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Saint Paul",
      "address_1": "2575 University Ave W",
      "reason_for_recall": "Synovis, a subsidiary of Baxter International Inc., is recalling certain shipments of VASCUGUARD and DURA-GUARD because Synovis, a subsidiary of Baxter International Inc., is recalling certain shipments of VASCUGUARD and DURA-GUARD because the shipping configurations in which the 6 fluid ounce units containing a specific revision of the Instructions for Use (IFU) shipped in a divided cell shipping",
      "address_2": "",
      "product_quantity": "446 units",
      "code_info": "Lot Numbers:    SPCE113-03C0006  SPCE113-04D0002  SPCE113-04D0047  SPCE113-05E0052  SPCE113-05E0072  SPCE113-07G0077  SPCE113-08H0018  SPCE113-08H0073  SPCE113-03C0008  SPCE113-03C0072  SPCE113-04D0036  SPCE113-04D0092  SPCE113-04D0093  SPCE113-05E0047  SPCE113-05E0048  SPCE113-06F0053  SPCE113-06F0054  SPCE113-07G0008  SPCE113-07G0072  SPCE113-08H0016  SPCE113-FEB0092  SPCE113-JAN0046  SPCE113-JAN0106  SPCE113-03C0004  SPCE113-03C0069  SPCE113-03C0070  SPCE113-03C0071  SPCE113-04D0085  SPCE113-04D0086  SPCE113-05E0073  SPCE113-05E0074  SPCE113-06F0055  SPCE113-06F0057  SPCE113-06F0138  SPCE113-06F0139  SPCE113-07G0074  SPCE113-07G0075  SPCE113-08H0019  SPCE113-JAN0047  SPCE113-JAN0048  SPCE113-JAN0109  SPCE113-JAN0125",
      "center_classification_date": "20131118",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "MN",
      "product_description": "Dura Guard, Dural Repair Patch with Apex Processing.    For use as a dura substitute for the closure of dura mater during neurosurgery.    Product Code:    DG0209SN    DG0209SN     DG0209SN    DG0209SN     DG0209SN      DG0209SN      DG0209SN     DG0209SN     DG0404SN       DG0404SN       DG0404SN      DG0404SN      DG0404SN      DG0404SN      DG0404SN       DG0404SN      DG0404SN   DG0404SN     DG0404SN     DG0404SN    DG0404SN       DG0404SN      DG0404SN     DG0608SN      DG0608SN       DG0608SN      DG0608SN     DG0608SN    DG0608SN       DG0608SN       DG0608SN       DG0608SN      DG0608SN      DG0608SN     DG0608SN     DG0608SN        DG0608SN        DG0608SN    DG0608SN      DG0608SN      DG0608SN      DG0608SN",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synovis Surgical Innovations, Inc.",
      "recall_number": "Z-0339-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66763",
      "termination_date": "20140603",
      "more_code_info": "",
      "recall_initiation_date": "20131028",
      "postal_code": "55114-1073",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}