{
  "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": {
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      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85124",
      "recalling_firm": "OriGen Biomedical, Inc.",
      "address_1": "7000 Burleson Rd Bldg D",
      "address_2": "N/A",
      "postal_code": "78744-3202",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "US: TX",
      "recall_number": "Z-0318-2021",
      "product_description": "3/8\" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only",
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      "center_classification_date": "20201030",
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      "report_date": "20201111",
      "code_info": "Lot # 042417-5045"
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}