{
  "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": "Terminated",
      "city": "Medford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64069",
      "recalling_firm": "Allergen Medical",
      "address_1": "200 Boston Avenue",
      "address_2": "N/A",
      "postal_code": "02155",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA including the states of CA, FL, GA, MI, MN, NJ, NY, OH, OR, RI, TX, VA, and WA, and the countries of Germany, Spain, and UK.",
      "recall_number": "Z-0794-2013",
      "product_description": "SeriScaffold Surgical Scaffold  Product Number: SCF10X25AGEN.    Surgical mesh for use in open or laparoscopic procedures.",
      "product_quantity": "225 units (US) and 81 (Outside US)",
      "reason_for_recall": "Product is dual packaged in an inner and outer pouch, the outer pouch seal may be compromised and sterility may not be assured",
      "recall_initiation_date": "20130108",
      "center_classification_date": "20130207",
      "termination_date": "20130729",
      "report_date": "20130213",
      "code_info": "Lot Numbers:   P2012040901 (US)  P2011080101B and P2011090901A (Outside the US)",
      "more_code_info": ""
    }
  ]
}