{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mansfield",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84591",
      "recalling_firm": "PediaLift LLC",
      "address_1": "181 Illinois Ave S",
      "address_2": "N/A",
      "postal_code": "44905-2825",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "The products were distributed to the following US states:  IN, NJ, NY, OH, and PA",
      "recall_number": "Z-0931-2020",
      "product_description": "PediaLift Access Device, Device Identifier: B751PDLFT0",
      "product_quantity": "11",
      "reason_for_recall": "The firm was unsuccessful in obtaining a satisfactory Certificate of   Conformance from the original vendor of the mattress showing that they are in compliance with labeling requirements.",
      "recall_initiation_date": "20190703",
      "center_classification_date": "20200201",
      "termination_date": "20200515",
      "report_date": "20200212",
      "code_info": "Serial Numbers: PCL-HDPE-DL-1, PCL-HDPE-DL-2, PCL-HDPE-DL-3, PCL-HDPE-DL-4, PCL-HDPE-DL-5, PCL-HDPE-DL-6, PCL-HDPE-DL-7, PCL-HDPE-DL-8, PCL-HDPE-DL-9, PCL-HDPE-DL-10, PCL-HDPE-DL-11, PCL-HDPE-DL-12"
    }
  ]
}