{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Westborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81454",
      "recalling_firm": "GE Healthcare Biosciences",
      "address_1": "14 Walkup Dr",
      "address_2": "N/A",
      "postal_code": "01581-1019",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide Distribution",
      "recall_number": "Z-0388-2019",
      "product_description": "DeltaVision OMX SR Imaging System Model Number: 29115476     The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal Reflection Fluorescence and localization microscopy may be used to examine a variety of samples over long periods of time.",
      "product_quantity": "39",
      "reason_for_recall": "Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.",
      "recall_initiation_date": "20180910",
      "center_classification_date": "20181120",
      "termination_date": "20200512",
      "report_date": "20181128",
      "code_info": "System Serial number OM20072 - OM40122",
      "more_code_info": ""
    }
  ]
}