{
  "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": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84272",
      "recalling_firm": "Abbott Medical",
      "address_1": "5050 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-3209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "nationwide",
      "recall_number": "Z-0664-2020",
      "product_description": "Radiofrequency Grounding Pad, REF RF-DGP-L",
      "product_quantity": "8940 devices",
      "reason_for_recall": "Affected lots were manufactured with the protective release liner in an incorrect orientation.  When attempting to remove this disposable release liner, a clear film may be left on the grounding pad which may interfere with patient skin contact and lead to uneven heating.",
      "recall_initiation_date": "20191014",
      "center_classification_date": "20191210",
      "termination_date": "20210719",
      "report_date": "20191218",
      "code_info": "UDI:  05415067028914  Batch Numbers:  810319004, 810319005, and 810319021",
      "more_code_info": ""
    }
  ]
}