{
  "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": "Powell",
      "address_1": "200 Debusk Ln",
      "reason_for_recall": "One lot of eye spears was labeled as being x-ray detectable, but contained non x-ray detectable product.",
      "address_2": "",
      "product_quantity": "726 cases (7242 units)",
      "code_info": "Lot Number 32794811",
      "center_classification_date": "20131114",
      "distribution_pattern": "Nationwide Distribution",
      "state": "TN",
      "product_description": "DeRoyal (R) Surgical Eye Spears, REF 30-049, Sterile EO, Manufacturer:  DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN  37849, MADE IN GUATEMALA    cleaning of fluids from surgical site in or near the eye",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "DeRoyal Industries Inc",
      "recall_number": "Z-0275-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66608",
      "termination_date": "20140804",
      "more_code_info": "",
      "recall_initiation_date": "20130812",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}