{
  "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": "San Antonio",
      "address_1": "4350 Lockhill Selma Rd",
      "reason_for_recall": "The voluntary recall is due to the needle set not meeting its specifications.",
      "address_2": "Suite 150",
      "product_quantity": "172",
      "code_info": "Part number 9079-VC-005; lot code 3606455",
      "center_classification_date": "20140922",
      "distribution_pattern": "Worldwide Distribution-US (nationwide) including the states of LA, NY, CA, CT, WA, AK, NJ, TX, GA, MI, MO, MD, FL, KY, VA, OH, UT, SC, NC, IN, AZ, MN, IL, TN, OK, KS, NE, MT, MS, AR, ID, WV and PA., and Internationally to Canada",
      "state": "TX",
      "product_description": "EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455",
      "report_date": "20141001",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vidacare Corporation",
      "recall_number": "Z-2672-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67912",
      "termination_date": "20150130",
      "recall_initiation_date": "20140331",
      "postal_code": "78249-2162",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}