{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Maple Grove",
      "address_1": "11400 73rd Ave N",
      "reason_for_recall": "Sterilmed, a division of Johnson & Johnson Medical NV/SA (Sterilmed), has become aware of an issue affecting certain lots of Reprocessed SOUNDSTAR® eco Diagnostic Ultrasound Catheters for which Sterilmed is the reprocessor and Biosense Webster is the distributor. Sterilmed determined that the units of these lots were incorrectly processed and as a result when the affected catheter is conne",
      "address_2": "",
      "product_quantity": "22",
      "code_info": "Lot Numbers: 1717945, 1721574, 1721575 and 1723123    Catalog Nos: M-5723-115, Model Number BIO10438577",
      "center_classification_date": "20141009",
      "distribution_pattern": "US Distribution including the states of WA and CA.",
      "state": "MN",
      "product_description": "Biosense Webster's Reprocessed SOUNDSTAR¿ eco Diagnostic Ultrasound Catheters, Catalog Nos: M-5723-115, Model Number BIO10438577.",
      "report_date": "20141015",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "STERILMED, INC.",
      "recall_number": "Z-0059-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69337",
      "termination_date": "20150811",
      "more_code_info": "",
      "recall_initiation_date": "20140924",
      "postal_code": "55369-5561",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}