{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "West Chester",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98754",
      "recalling_firm": "Aniara Diagnostica LLC",
      "address_1": "7768 Service Center Dr",
      "address_2": "",
      "postal_code": "45069-2442",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, GA, MN, MO, NC, NM, NY, VA, WA, and WI",
      "recall_number": "Z-2171-2026",
      "product_description": "ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A",
      "product_quantity": "359 units",
      "reason_for_recall": "Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.",
      "recall_initiation_date": "20260401",
      "center_classification_date": "20260512",
      "report_date": "20260520",
      "code_info": "UDI-DI: 03663537018763; Lot Number: FD1265",
      "more_code_info": ""
    }
  ]
}