{
  "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": {
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      "city": "Peoria",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88751",
      "recalling_firm": "Scrip Inc",
      "address_1": "9005 N Industrial Rd",
      "address_2": "N/A",
      "postal_code": "61615-1511",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution to all 50 states.",
      "recall_number": "Z-0224-2022",
      "product_description": "Scrip Ultrasound Gel Clear, 5L  Intended for use in acoustic coupling of ultrasound transducer to tissue",
      "product_quantity": "1001 gallons",
      "reason_for_recall": "Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.",
      "recall_initiation_date": "20210818",
      "center_classification_date": "20211117",
      "report_date": "20211124",
      "code_info": "Item Number: 663 0061, all lots bearing old style logo.  Older logo states that product was manufactured by Eco-Med Pharmaceuticals in Canada.",
      "more_code_info": ""
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}