{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Temecula",
      "address_1": "26531 Ynez Rd",
      "reason_for_recall": "The recall was initiated because Abbot Vascular has discovered that the identified lots of the RX Accunet Embolic Protection System may exhibit difficult removal of the peel away sheath due to higher than normal wall thickness.",
      "address_2": "",
      "product_quantity": "1253 units (962 units in the US & Puerto Rico)",
      "code_info": "Lot Number:  1081061, 1082561, 1091361, 1080561, 1081761, 1090261, 1091561, 1100461, 1080361, 1081661, 1090161, 1090861, 1092361, 1080861, 1082661, 1100761, 1081761, 1092861, 1082461, 1081161, 1082261, 1083061, 1081961, 1093061.",
      "center_classification_date": "20130131",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Austria, Belgium, China, Germany, Spain, France, United Kingdom, Italy, Pakistan, Poland, Russia, Slovakia, Taiwan, and South Africa.",
      "state": "CA",
      "product_description": "Brand Name: RX Accunet Embolic Protection System  Common Name: RX Accunet EPS.    Part Numbers: 101649-45, 1011649-55, 1011649-65, 1011649-75, 1011650-55, 1011650-65, 1011651-45, 1011651-55.    The RX Accunet EPS is indicated for use as a guide wire and embolic protection system.",
      "report_date": "20130206",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Vascular",
      "recall_number": "Z-0757-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "60906",
      "termination_date": "20130131",
      "more_code_info": "",
      "recall_initiation_date": "20111130",
      "postal_code": "92591-4630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}