{
  "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": "Mislabeled:  The 8\" x 10\" package contains 7\" x 9\" VENTRALIGHT ST Mesh product and the 7\" x 9\" package contains 8\" x 10\"  VENTRALIGHT ST Mesh product",
      "address_2": "",
      "product_quantity": "49 units",
      "code_info": "Lot # HUWE1779",
      "center_classification_date": "20120920",
      "distribution_pattern": "Nationwide Distribution.",
      "state": "RI",
      "product_description": "Bard Ventralight ST Mesh. - Ellipse 8\" x 10\" (20.3 cm x 25.4 cm)   Product Code 5954810.     The Bard Ventralight ST Mesh is a dual-component (absorbable and nonabsorbable) sterile prosthesis. The device classification name is \"Mesh, Surgical, Polymeric.\" It is in tented for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.",
      "report_date": "20120926",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Davol, Inc., Subs. C. R. Bard, Inc.",
      "recall_number": "Z-2412-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63069",
      "termination_date": "20130903",
      "more_code_info": "",
      "recall_initiation_date": "20120904",
      "postal_code": "02886-2850",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}