{
  "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": [
    {
      "status": "Ongoing",
      "city": "Somerville",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67736",
      "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": "US Distribution including the states of FL, NJ, MO, IL, PA, NC. TX, TN, WA, ID, UT, WV, MS. CA, AL, MA. GA, LA and OK.",
      "recall_number": "Z-1329-2014",
      "product_description": "Proceed Surgical Mesh, Product Codes PCDB1, PCDT1, and PCDJ1.       Ethicon Inc., Johnson & Johnson Medical GmbH, used for the repair of hernias and other fascial deficiencies that require the addition of a reinforcing or bridging material to obtain the desired surgical result.",
      "product_quantity": "223 units",
      "reason_for_recall": "The possibility exists that an incomplete seal on the packaging compromised the sterility of the device and introduced the potential for delamination.",
      "recall_initiation_date": "20140219",
      "center_classification_date": "20140403",
      "report_date": "20140409",
      "code_info": "Product Code PCDB1 - Lot number - GGG157  Product Code PCDT1 - Lot number - GGG158  Product Code PCDJ1 - Lot number  -GGG159"
    }
  ]
}