{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Boerne",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89829",
      "recalling_firm": "Stanbio Laboratory, LP",
      "address_1": "1261 N Main St",
      "address_2": "N/A",
      "postal_code": "78006-3014",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution CA, TX, OK, SD, IL, NV, MO, FL, WA, KY, WI, PA, NC, GA, MD, MN",
      "recall_number": "Z-0905-2022",
      "product_description": "Separation Technology Creamatocrit Plus, Catalog Number: 100-146",
      "product_quantity": "50",
      "reason_for_recall": "The device was being marketed as an IVD without a 510(k). Therefore, performance characteristics of these breast milk analyzers have not been adequately validated.  An erroneous result could lead to sub-optimal nutrition supplementation for patients (infants)",
      "recall_initiation_date": "20220316",
      "center_classification_date": "20220411",
      "termination_date": "20250102",
      "report_date": "20220420",
      "code_info": "Sold between 2019 and 2021"
    }
  ]
}