{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warwick",
      "address_1": "100 Crossings Blvd",
      "reason_for_recall": "The patient record peel-off label product code and size did not match the other labeling and actual product in the packaging for the Bard Small PerFix Light Plug.",
      "address_2": "",
      "product_quantity": "78 units",
      "code_info": "Lot# HUYD0176",
      "center_classification_date": "20141107",
      "distribution_pattern": "US Distribution including the states of CA, NM, OH, DE, MN, UT, MD and MO.",
      "state": "RI",
      "product_description": "Bard¿ PerFix Light Plug      The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects.",
      "report_date": "20141119",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Davol, Inc., Subs. C. R. Bard, Inc.",
      "recall_number": "Z-0191-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69464",
      "termination_date": "20151223",
      "more_code_info": "",
      "recall_initiation_date": "20141008",
      "postal_code": "02886-2850",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}