{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lenexa",
      "state": "KS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95458",
      "recalling_firm": "Remel, Inc",
      "address_1": "12076 Santa Fe Trail Dr",
      "address_2": "N/A",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to IL, IN, MN, NE, SD, TX, VA, and WA.  There was government distribution but no military distribution.  Foreign distribution was made to the United Kingdom.",
      "recall_number": "Z-0266-2025",
      "product_description": "remel BactiDrop Acridine Orange, REF 21502, 50 per package.",
      "product_quantity": "29 kits",
      "reason_for_recall": "A color change of the solution within the dropper can occur from orange-yellow to light yellow resulting in out-of-specification fluorescent stain results.",
      "recall_initiation_date": "20240920",
      "center_classification_date": "20241030",
      "report_date": "20241106",
      "code_info": "Lot 733100, Exp. 2025-04-04; UDI-DI 848838000447.",
      "more_code_info": ""
    }
  ]
}