{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97128",
      "recalling_firm": "Drs Vascular, Inc",
      "address_1": "1914 Otoole Way",
      "address_2": "N/A",
      "postal_code": "95131-2237",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "U.S. Nationwide distribution in the states of AR, CA, and NY.",
      "recall_number": "Z-2330-2025",
      "product_description": "Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Description: The DRS Vascular Q-Stop Suture Retention Appliance is a sterile, single-use, lightweight device made of biocompatible materials that can be easily installed within minutes to assist with venous access hemostasis. Component: No",
      "product_quantity": "264",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20250516",
      "center_classification_date": "20250815",
      "report_date": "20250827",
      "code_info": "Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402"
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}