{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "West Sacramento",
      "address_1": "2040 Enterprise Blvd",
      "reason_for_recall": "Technical Support Bulletin issued in February 2013 did not mention performance limitation for Proteus mirabilis and Imp when using the CLSIM100-S20 revised interpretive criteria.",
      "address_2": "",
      "product_quantity": "Approx ~(216240 boxes U.S. and 84249 boxes OUS)  total",
      "code_info": "Catalog number: B1017-412; Siemens Material Number (SMN):   10371535.",
      "center_classification_date": "20150427",
      "distribution_pattern": "Worldwide Distribution: US (Nationwide) and to countries of: Argentina, Bahamas, Brazil, Canada, China, Ecuador, Egypt, Germany, Lithuania, Mexico, Paraguay, Peru Poland, Portugal, Romania, Russian Federation, Singapore, South Africa, Spain, Taiwan, Thailand, Trinidad and Tobago, United Arab Emirates, Uruguay, and Venezuela.",
      "state": "CA",
      "product_description": "MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels  Containing Lower Imipenem Dilutions for Reporting CLSI M100-S20  Breakpoints  Panel: Neg MIC 38, Catalog B1017-412    Microbiology: For use with MicroScan Dried Gram  Negative MIC/Combo Panels and Dried Gram Negative Breakpoint Combo Panels. MicroScan panels are designed  for use in determining antimicrobial agent susceptibility and/or identification to the  species level of aerobic and facultatively anaerobic gram-negative bacilli.",
      "report_date": "20150506",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Beckman Coulter, Inc.",
      "recall_number": "Z-1533-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70893",
      "termination_date": "20150427",
      "more_code_info": "",
      "recall_initiation_date": "20140808",
      "postal_code": "95691-3427",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}