{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72274",
      "recalling_firm": "Integra LifeSciences Corp. d.b.a. Integra Pain Management",
      "address_1": "3498 West 2400 South #1050",
      "address_2": "N/A",
      "postal_code": "84119",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distributed to the state of : MD.",
      "recall_number": "Z-0193-2016",
      "product_description": "Integra¿ Bone Marrow Biopsy Trays Catalogue No. 3404253  Various medical devices and components used to perform bone marrow biopsies are placed in a plastic tray which is sealed in an EtO sterilizable pouch.  Vials of 1 % Lidocaine HCL Injection, USP, 10 mg/mL (manufactured and distributed by Hospira Inc.) are placed in a separate sealed pouch.  After the bone marrow biopsy pouch is sterilized, a Lidocaine pouch is affixed to each.  Ten of these pouches are inserted in a sealed and labeled corrugated box.",
      "product_quantity": "A total of 470 packages (47 cases)",
      "reason_for_recall": "Integra received an Urgent Drug Recall Notice from Hospira Inc. for their 1% Lidocaine HCL Injection, USP, 10 mg/mL, Lot 44-359-DK.  Hospira Inc. is recalling vials of Lot 44-359-DK, 1% Lidocaine HCL Injection, USP, 10 mg/mLm distributed by Hospira from February 2015 to March 2015 due to a confirmed complaint of visible, partially embedded particulate within a single-dose glass teartop vial.",
      "recall_initiation_date": "20150922",
      "center_classification_date": "20151029",
      "termination_date": "20160129",
      "report_date": "20151104",
      "code_info": "There are 3 Integra Lot Numbers affected by the recall of the single lot of Hospira Lidocaine:  W1501193, W1504141, W1505078  Catalogue No. 3404253"
    }
  ]
}