{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Republic",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88210",
      "recalling_firm": "ROi CPS LLC",
      "address_1": "3000 E Sawyer Rd",
      "address_2": "",
      "postal_code": "65738-2758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Missouri",
      "recall_number": "Z-2168-2021",
      "product_description": "Regard NEWBORN KIT, LD00201K, Item Number:  830016011.  Medical convenience kit which includes an infant heel warmer.",
      "product_quantity": "688 units",
      "reason_for_recall": "Instructions for use updated to include the following cautionary statement for the heel warmer, \"Activate away from the user's face and away from the infant and others.\"",
      "recall_initiation_date": "20210614",
      "center_classification_date": "20210730",
      "termination_date": "20230308",
      "report_date": "20210811",
      "code_info": "Lot Numbers:  77906K, 78673K, 79327K, 80825K",
      "more_code_info": ""
    }
  ]
}