{
  "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": "Terminated",
      "city": "Cincinnati",
      "state": "OH",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88540",
      "recalling_firm": "Athena Medical Products Inc",
      "address_1": "11270 Groome Rd St # B",
      "address_2": "N/A",
      "postal_code": "45242",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to one distributor within the US.",
      "recall_number": "Z-2392-2021",
      "product_description": "LiquaSonic Ultrasound Gel 5L, Model No. 001222",
      "product_quantity": "480 cases of 4",
      "reason_for_recall": "Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.",
      "recall_initiation_date": "20210820",
      "center_classification_date": "20210909",
      "termination_date": "20230202",
      "report_date": "20210915",
      "code_info": "UDI 00856589006137, All lot codes. Product will be discontinued and will not be reintroduced.",
      "more_code_info": ""
    }
  ]
}