{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Saint Louis",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88195",
      "recalling_firm": "LIEBEL-FLARSHEIM COMPANY LLC",
      "address_1": "1034 S Brentwood Blvd",
      "address_2": "",
      "postal_code": "63117-1223",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution and in the country of Canada",
      "recall_number": "Z-1992-2021",
      "product_description": "HydraVision Digital Imaging System  Product ID/Reorder Number: 705559 (65KW)",
      "product_quantity": "17",
      "reason_for_recall": "Failure to comply with the performance standard for fluoroscopy systems. Per 21 CFR 1020.32(k)(6), the displayed AKR and cumulative air kerma shall not deviate from the actual values by more than ¿ 35 percent. The dosage displayed on the generator console and table display (monitor) is higher than the actual delivered dose.",
      "recall_initiation_date": "20210311",
      "center_classification_date": "20210702",
      "termination_date": "20240918",
      "report_date": "20210714",
      "code_info": "Product ID/Reorder Number: 705559 (65KW), 705560 (80KW)  Model/NDC: HUTSHVDIS",
      "more_code_info": ""
    }
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}