{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fairfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79910",
      "recalling_firm": "Parker Laboratories, Inc.",
      "address_1": "286 Eldridge Rd",
      "address_2": "N/A",
      "postal_code": "07004-2509",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "The products were distributed to the following US states: CA, FL, GA, IA, IL, OH, TN, and VA.  The products were distributed to the following foreign countries: Canada, United Kingdom, and Malta.",
      "recall_number": "Z-1777-2018",
      "product_description": "Sterile Aquasonic 100 Ultrasound Transmission Gel, 20 grams, Model Number 01-01-4, 400 packets/case",
      "product_quantity": "3275 cases/1310000 packets",
      "reason_for_recall": "There is a potential for the gel packets to have leaks in the packet seal.",
      "recall_initiation_date": "20170413",
      "center_classification_date": "20180509",
      "termination_date": "20201026",
      "report_date": "20180516",
      "code_info": "Lot numbers: L0117006, L0117007, L0217001, L0217002, L0217004, L0217006"
    }
  ]
}