{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25288",
      "product_res_number": "Z-0462-03",
      "event_date_initiated": "2002-01-25",
      "event_date_posted": "2003-01-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-11-17",
      "res_event_number": "25139",
      "product_code": "JAJ",
      "product_description": "Novoste, Beta-Cath 3.5F System, New B-Rail 3.5F Delivery Catheter,  with Indicator of Source Train (IST), Novoste Corporate, 3890 Steve Reynolds Blvd, Norcross, GA 30093, Tel: +1770-717-0904, Fax: +1770-717-1283, 1-800-NOVOSTE (1-800-668-6783), www.novoste.com.",
      "code_info": "Catalog Numbers: TDA-0030 - Serial Numbers: 81431, 81761, 82548, 83007, 83926, 84395, 85014, 85021, 86333, 86489, 86874, 86889, 86897, 87097, 87103, 87189, 88592, 88692, 88734, 88738, 89035, 89037, 89058,  TDA-0040- Serial Numbers: 77252, 81012, 83214, 85327, 87816, 87834, 88591, 88598, 88617, 88622, 88626, 88632, 88681, 88697, 88691, 88697, 88702, 88712, 88718, 88719, 88720, 88721, 88736, 88739, 89045, 89049, 89054.",
      "firm_fei_number": "3000205626",
      "recalling_firm": "Novoste Corporation",
      "address_1": "3890 Steve Reynolds Blvd.",
      "city": "Norcross",
      "state": "GA",
      "postal_code": "30093",
      "additional_info_contact": "Mr. Adam G. Lowe\n770-717-0904",
      "reason_for_recall": "Mislabeling.  Source calibrated incorrectly, resultant dose rate lower than expected.",
      "root_cause_description": "Other",
      "action": "Customers were notified via Advisory Letter followed up with a Recall Letter and Customer Informational Letter on/about January 24, 2002. Customers were advised to discontinue use of the product and return the affected product to Novoste Corp. to be recalibrated to obtain a correct calibration certificate.",
      "product_quantity": "50 units",
      "distribution_pattern": "Nationwide.  (AR, AZ, CA, FL, GA, IA, ID, IL, KY, MD, MI, MN, MO, NC, NM, NV, NY, OH, PA, TN, TX, VA, WA). No foreign or government accounts involved.",
      "openfda": {}
    }
  ]
}