{
  "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": [
    {
      "status": "Terminated",
      "city": "Brighton",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89316",
      "recalling_firm": "FlexDex Inc.",
      "address_1": "10421 Citation Dr Ste 900",
      "address_2": "",
      "postal_code": "48116-6558",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "",
      "recall_number": "Z-0531-2022",
      "product_description": "8mm FlexDex Needle Driver, Product Code FD-335 ND",
      "product_quantity": "273",
      "reason_for_recall": "The firm is reinforcing the IFU instructions: \"Do not use if the package is damaged.\" If upon inspection of the packaging, any damage is observed, including pinholes or tears in the pouch, the product should not be used.",
      "recall_initiation_date": "20211222",
      "center_classification_date": "20220127",
      "termination_date": "20230725",
      "report_date": "20220202",
      "code_info": "All lots",
      "more_code_info": ""
    }
  ]
}