{
  "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": [
    {
      "country": "United States",
      "city": "Columbus",
      "address_1": "585 Cleveland Ave",
      "reason_for_recall": "a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.",
      "address_2": "",
      "product_quantity": "13440 cartons but only 550 cartons (6600 bottles) affected",
      "code_info": "Carton Batch # 06108XK00; Bottle Batch # 02567X800",
      "center_classification_date": "20190911",
      "distribution_pattern": "Distribution Centers in:  Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin",
      "state": "OH",
      "product_description": "Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Nutrition, Division of Abbott Laboratories",
      "recall_number": "F-2153-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Food",
      "event_id": "83608",
      "termination_date": "20191204",
      "more_code_info": "",
      "recall_initiation_date": "20190816",
      "postal_code": "43215-1755",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}