{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Santa Clara",
      "address_1": "5452 Betsy Ross Dr",
      "reason_for_recall": "A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.",
      "address_2": "",
      "product_quantity": "55 units",
      "code_info": "Lot No: F1609702, Expiry 4/20/2018; Lot No. F1534302, Expiry 12/31/2016",
      "center_classification_date": "20160803",
      "distribution_pattern": "US in the states of CA, and MS.",
      "state": "CA",
      "product_description": "6F/7F MynxGrip Vascular Closure Device;  Product Model MX6721,    Product Usage:  The 6F/7F MynxGrip Vascular Closure Device is indicated for use to seal femoral arterial and femoral venous access sites while reducing times to hemostasis and ambulation in patients who have undergone diagnostic or interventional endovascular procedures utilizing a 6F or 7F procedural sheath. The 6F/7F MynxGrip Vascular Closure Device is designed to achieve femoral artery and femoral vein hemostasis via delivery of an extravascular, water-soluble synthetic sealant using a balloon catheter in conjunction with a standard procedural sheath. The sealant is comprised of a polyethylene glycol (PEG) material which expands upon contact with subcutaneous fluids to seal the arteriotomy or venotomy. The sealant is resorbed by the body within 30-days.",
      "report_date": "20160810",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AccessClosure, Inc., A Cardinal Health Company",
      "recall_number": "Z-2329-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74599",
      "termination_date": "20160815",
      "more_code_info": "",
      "recall_initiation_date": "20160713",
      "postal_code": "95054-1101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}