{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Tempe",
      "address_1": "1625 W 3rd St Bldg 1",
      "reason_for_recall": "Complaints received that products packaged with the incorrect introducer sheath size.",
      "address_2": "",
      "product_quantity": "900 units",
      "code_info": "Product Code: 1808060  Device Listing Number: D004935  UDI: (01)00801741027031(17)191130(10)RECS2407  Lot Number: RECS2407",
      "center_classification_date": "20191127",
      "distribution_pattern": "US - Nationwide    OUS - None",
      "state": "AZ",
      "product_description": "PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter",
      "report_date": "20191204",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "recall_number": "Z-0582-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84169",
      "more_code_info": "",
      "recall_initiation_date": "20190214",
      "postal_code": "85281-2438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
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}