{
  "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-0647-2023",
      "product_description": "DeRoyal MYELOGRAM PACK, REF 89-9304.05",
      "product_quantity": "2280 kits",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20221103",
      "center_classification_date": "20221215",
      "report_date": "20221221",
      "code_info": "Lot Numbers:  Lot 55612944 exp 3/1/2026; Lot 56615881 exp 7/1/2026; Lot 56279557 exp 5/1/2026; Lot 57185350 exp7/1/2026; Lot 57591593 exp 1/1/2025"
    }
  ]
}