{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Somerville",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86631",
      "recalling_firm": "Ethicon, Inc.",
      "address_1": "Us Highway 22 West",
      "address_2": "N/A",
      "postal_code": "08876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The impacted lot (295 units) was distributed to 27 countries worldwide excluding the US. However, the firm is only recalling the 15 units that were distributed in South Korea due to South Korea's Ministry of Food and Drug Safety (MFDS) requirements.",
      "recall_number": "Z-0533-2021",
      "product_description": "PROCEED Surgical Mesh  Hernia Mesh Oval, 15 cm x 20 cm",
      "product_quantity": "295 units distributed. Only 15 units are being recalled.",
      "reason_for_recall": "The firm is recalling the PROCEED Surgical Mesh device, because it is a sterile device, and a customer found a hair inside of the primary packaging of a single unit.",
      "recall_initiation_date": "20201023",
      "center_classification_date": "20201203",
      "termination_date": "20221221",
      "report_date": "20201209",
      "code_info": "Product Code - PCDG1  Product Lot - PHG118  GTIN Code - 10705031047716  Expiration Date: 07/31/2021",
      "more_code_info": ""
    }
  ]
}