{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Maryland Heights",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76351",
      "recalling_firm": "ErgoSafe Products, LLC (DBA) Prism Medical",
      "address_1": "10888 Metro Ct",
      "address_2": "N/A",
      "postal_code": "63043-2413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed to MT and NV; one VA consignee.",
      "recall_number": "Z-1406-2017",
      "product_description": "A-series lift - A625 Manual Part No. 324117. Prism Medical.",
      "product_quantity": "76",
      "reason_for_recall": "During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.",
      "recall_initiation_date": "20170130",
      "center_classification_date": "20170303",
      "termination_date": "20171204",
      "report_date": "20170315",
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