{
  "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": "Ongoing",
      "city": "Powell",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91134",
      "recalling_firm": "DeRoyal Industries Inc",
      "address_1": "200 Debusk Ln",
      "address_2": "N/A",
      "postal_code": "37849-4703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US:  Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi",
      "recall_number": "Z-0715-2023",
      "product_description": "DeRoyal CATARACT PACK, REF 89-10086.05",
      "product_quantity": "520 kits",
      "reason_for_recall": "DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.",
      "recall_initiation_date": "20221103",
      "center_classification_date": "20221215",
      "report_date": "20221221",
      "code_info": "Lot Numbers: 57003552 exp 09/01/2024; 57467226 exp 12/01/2024; 55748075 exp *; 56250244 exp *; 57899344 exp *; 57913353 exp *"
    }
  ]
}