{
  "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": "Temecula",
      "address_1": "26531 Ynez Rd",
      "reason_for_recall": "Incorrect expiration being entered for one lot.",
      "address_2": "",
      "product_quantity": "26 units",
      "code_info": "Device Identifier #: 08717648 01360 7  Part Number: 1000185  Lot number: 60047593",
      "center_classification_date": "20190226",
      "distribution_pattern": "US Nationwide Distribution - NC and NY",
      "state": "CA",
      "product_description": "PLUS 30 PRIORITY PACK Accessory Kit    Product Usage:  Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).",
      "report_date": "20190306",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Vascular",
      "recall_number": "Z-0960-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82015",
      "more_code_info": "",
      "recall_initiation_date": "20180703",
      "postal_code": "92591-4630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}