{
  "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": "Salt Lake City",
      "address_1": "3498 West 2400 South #1050",
      "reason_for_recall": "A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged and labeled as 18 Gauge, 5 inch needles.",
      "address_2": "",
      "product_quantity": "90 Tuohy needles (9 cases of 10 each)",
      "code_info": "Lot No. W1412086, Exp DEC-2017.",
      "center_classification_date": "20150428",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "UT",
      "product_description": "Integra Long Epidural Steroid Injection Needle (Tuohy Needle), 18 Gauge x 5 inch Removable Wing, Metal Stylet, Calibrations (10BX), Catalogue No. PITRW1850.    Used to administer steroid medication in the epidural space.",
      "report_date": "20150506",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Integra LifeSciences Corp. d.b.a. Integra Pain Management",
      "recall_number": "Z-1544-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70873",
      "termination_date": "20150624",
      "more_code_info": "",
      "recall_initiation_date": "20150330",
      "postal_code": "84119",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}