{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Richmond",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97185",
      "recalling_firm": "Spark Biomedical Inc",
      "address_1": "19830 Fm 1093 Rd Ste 401",
      "address_2": "N/A",
      "postal_code": "77407-8621",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2287-2025",
      "product_description": "Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-320-K-28, 11-321-K-28",
      "product_quantity": "78 units",
      "reason_for_recall": "Due to manufacturing issue, neurostimulator device may experience  \"cable disconnect\" error message and interruption to stimulation output.",
      "recall_initiation_date": "20250702",
      "center_classification_date": "20250811",
      "report_date": "20250820",
      "code_info": "Lot numbers: V2408xxxx and runs through V2519xxxx UDI: 11-110/00850052017033; 11-310-K/00860005396948; 11-320-K/00860005396986; 11-321-K/00850052017163; 11-310-K-28/00850052017088; 11-320-K-28/00850052017071; 11-321-K-28/00850052017170",
      "more_code_info": ""
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}