{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Saint Cloud",
      "address_1": "200 Cooper Ave N",
      "reason_for_recall": "The recommended hydration fluid for the 8180 Gram-Positive Blood Culture Control Panel (Inactivated Pellet), has changed from sterile 0.85% saline or sterile blood culture media to sterile DI water or pH 7.2 phosphate buffer.",
      "address_2": "",
      "product_quantity": "810",
      "code_info": "Lot #  8180-46  8180-47  8180-48  8180-49  8180-50  8180-51  8180-52",
      "center_classification_date": "20200116",
      "distribution_pattern": "Distributed nationwide including Washington DC, and distributed internationally to Germany and Netherlands.",
      "state": "MN",
      "product_description": "Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180  Used in test systems to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation.",
      "report_date": "20200122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Microbiologics Inc",
      "recall_number": "Z-0812-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84524",
      "termination_date": "20201211",
      "more_code_info": "",
      "recall_initiation_date": "20191216",
      "postal_code": "56303-4440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}