{
  "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": "2026-04-08",
    "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": "80562",
      "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": "Distribution was nationwide.  There was military distribution and no government distribution.  Foreign distribution was made to Bolivia, Malaysia, Mexico, Papua New Guinea, Paraguay, Philippines, and Suriname.",
      "recall_number": "Z-2926-2018",
      "product_description": "Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series.  The firm name on the label for the HemoPoint H2 shows Manufactured by EKF-diagnostic GmbH, Germany.",
      "product_quantity": "2,804 devices",
      "reason_for_recall": "The US prong (type A) adapter plate may crack, break, or detach and remain in the electrical outlet exposing live electrical contacts.",
      "recall_initiation_date": "20180208",
      "center_classification_date": "20180824",
      "termination_date": "20200904",
      "report_date": "20180905",
      "code_info": "Serial number range of affected power adapters:   41800001-41804000"
    }
  ]
}