{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
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      "city": "Indianapolis",
      "state": "IN",
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      "product_type": "Devices",
      "event_id": "68294",
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1790-2014",
      "product_description": "Roche MODULAR ANALYTICS EVO Serum Work Area (SWA), Operator's Manual Software Version 08-02; Filter label:  Filter (N)  Mat. No 03149773001, Contents 1, 768-320 Filter (N).    Product Usage:  Fully automated immunoassay analyzer intended for the in-vitro quantitative/qualitative determination of analytes in body fluids.",
      "product_quantity": "462",
      "reason_for_recall": "Under certain conditions loose ProCell/CleanCell aspiration tube filters may cause:  consecutive discrepant results; sipper alarm; foam on reservoirs and system reagent alarms.",
      "recall_initiation_date": "20140521",
      "center_classification_date": "20140613",
      "termination_date": "20150604",
      "report_date": "20140625",
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