{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Fraser",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96823",
      "recalling_firm": "Healthmark Industries Co., Inc.",
      "address_1": "18600 Malyn Blvd",
      "address_2": "N/A",
      "postal_code": "48026-3496",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and Internationally to countries of: Canada, Malaysia.",
      "recall_number": "Z-1909-2025",
      "product_description": "Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010",
      "product_quantity": "250000 units",
      "reason_for_recall": "During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their investigation. Healthmark Industries conducted its own investigation and concluded that the Pre-filled Water Syringe had been improperly used outside of the intended purpose.",
      "recall_initiation_date": "20250502",
      "center_classification_date": "20250605",
      "report_date": "20250611",
      "code_info": "Lot Numbers: 200001 200002 200003 200004 200005 200006 200007 200008 200009 200010 200011 200012 200013"
    }
  ]
}