{
  "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": "Branchburg",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93514",
      "recalling_firm": "Zeus Scientific, Inc.",
      "address_1": "199 Evans Way",
      "address_2": "N/A",
      "postal_code": "08876-4600",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US States: CA, MA, MI, NJ, NY, TN, UT.",
      "recall_number": "Z-0602-2024",
      "product_description": "ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M",
      "product_quantity": "296 kits",
      "reason_for_recall": "The organization completed a product improvement process to the conjugate found within the certain ELISA kits.  This modification was not reviewed and approved by FDA prior to its implementation.",
      "recall_initiation_date": "20231031",
      "center_classification_date": "20231221",
      "report_date": "20231227",
      "code_info": "UDI: (01)00845533001748(17)240731(10)23030068 (01)00845533001755(17)241130(10)23060217 (01)00845533001779(17)241130(10)23060218; Lot Numbers: 23030068 23060217 23060218"
    }
  ]
}