{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88314",
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "address_1": "1625 W 3rd St Bldg 1",
      "address_2": "N/A",
      "postal_code": "85281-2438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S Nationwide Distribution in the states of .: AZ, CT, DC, FL, IL, MA, MI, MO, NY, OK, TX, and VA    O.U.S.: Australia, Belgium, China, EMEA, Japan, Mexico, Saudi Arabia, Singapore, Taiwan",
      "recall_number": "Z-2249-2021",
      "product_description": "TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm  TIN3015 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 15G x 79mm",
      "product_quantity": "1,200 device",
      "reason_for_recall": "Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.",
      "recall_initiation_date": "20210623",
      "center_classification_date": "20210811",
      "report_date": "20210818",
      "code_info": "Catalog Number/UDI:  TIN3018/(01)10885403043819(17)241031(10)0001330956;  TIN3015/(01)10885403043796(17)241031(10)0001331229;    Serial Numbers:  0001330956;  0001331229;"
    }
  ]
}