{
  "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": [
    {
      "status": "Terminated",
      "city": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76363",
      "recalling_firm": "Vascular Solutions, Inc.",
      "address_1": "6464 Sycamore Ct N",
      "address_2": "N/A",
      "postal_code": "55369-6032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of NH, ME, VT, NY, LA, MS, AL CA, IA, WA, OR, MD, DE, PA, NJ, ID, TX, OK, MO, WI, GA, FL, AR, OH, AZ.",
      "recall_number": "Z-1250-2017",
      "product_description": "GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide.     Product Usage:  The GrebSet micro-introducer kit is intended to facilitate the percutaneous placement of guidewires in the vascular system and for delivery of contrast media to vascular sites.",
      "product_quantity": "633",
      "reason_for_recall": "Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires that  have a shelf life shorter than the kit expiration date.",
      "recall_initiation_date": "20170112",
      "center_classification_date": "20170223",
      "termination_date": "20180418",
      "report_date": "20170301",
      "code_info": "Lot Numbers:  581212, 584392, 594115, 597202"
    }
  ]
}