{
  "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-0579-2023",
      "product_description": "DeRoyal SHOULDER PACK, REF 89-6830.13",
      "product_quantity": "876 kits",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20221103",
      "center_classification_date": "20221215",
      "report_date": "20221221",
      "code_info": "Lot Numbers:  Lot 56184005 exp 11/1/2023; Lot 56254392 exp 10/1/2023; Lot 56777927 exp 1/1/2024; Lot 57391031 exp 2/1/2024; Lot 57684204 exp 5/1/2024"
    }
  ]
}