{
  "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": "Grand Island",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80380",
      "recalling_firm": "Life Technologies, Corp.",
      "address_1": "3175 Staley Rd",
      "address_2": "N/A",
      "postal_code": "14072-2028",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution.  US states: CA, CO, CT,  FL, GA, MA, MD, PA, RI, UT, and WA.,  Canada, France, Great Britain, Japan, Korea, Netherlands, and Switzerland.",
      "recall_number": "Z-2545-2018",
      "product_description": "Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, Model Number 11965175.  Tissue and cell culture medium.",
      "product_quantity": "91",
      "reason_for_recall": "It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging into outer non-sterile dust cover packaging, and subsequently mold may grow in the pooled, leaked media.",
      "recall_initiation_date": "20180510",
      "center_classification_date": "20180725",
      "termination_date": "20200505",
      "report_date": "20180801",
      "code_info": "Lot: 1945238"
    }
  ]
}