{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Bowdoin",
      "address_1": "1201 Main St",
      "reason_for_recall": "An electrical sub-circuit was not properly connected. Its purpose is to eliminate the possibility of interference with proper performance of the Guideline 5 Main Processing Unit, if an ESD event (greater than 6kV) were to occur.",
      "address_2": "",
      "product_quantity": "6 units",
      "code_info": "Serial Numbers: 45695, 48871, 48873, 48874, 46195, 46198",
      "center_classification_date": "20200708",
      "distribution_pattern": "US Nationwide distribution including in the states of CA, NC, TN, TX, WA.",
      "state": "ME",
      "product_description": "FHC Guideline 4000 5.0 \tGL5 Main Processing Unit - Product Usage: intended to record and stimulate electrophysiological activity, as well as aid in the accurate placement of electrodes and other instruments.  Catalogue Number: C0215\t  UDI: 00873263006740",
      "report_date": "20200715",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "FHC, Inc.",
      "recall_number": "Z-2540-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85897",
      "termination_date": "20201102",
      "more_code_info": "",
      "recall_initiation_date": "20200617",
      "postal_code": "04287-7302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}