{
  "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": "2026-08-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99390",
      "recalling_firm": "Covidien, LP",
      "address_1": "60 Middletown Ave",
      "address_2": "",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and the countries of Australia, Austria, Belgium, Bulgaria, Canada, Canary Islands, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Guadeloupe, Guatemala, Honduras, Hong Kong, Hungary, Iceland, India, Ireland, Israel, Italy, Japan, Kosovo, Lebanon, Lithuania, Luxembourg, Mexico, Namibia, Netherlands, North Macedonia, Northern Ireland, Norway,  Oman, Panama, Poland, Portugal, Qatar, Reunion, Romania, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland,  Taiwan, Thailand, Ukraine, United Arab Emirates, United Kingdom, Uzbekistan.",
      "recall_number": "Z-2920-2026",
      "product_description": "Dermalon    88861757-31 DERMALON* 4-0 BLU 75CM C13\t  \t88861757-31    88861799-31 DERMALON* 4-0 BLU 75CM C14\t  \t88861799-31",
      "product_quantity": "135,875 total",
      "reason_for_recall": "Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.",
      "recall_initiation_date": "20260624",
      "center_classification_date": "20260807",
      "report_date": "20260819",
      "code_info": "88861757-31    UDI-DI 10884521070912    Lot D6A3020FY  UDI-DI 20884521070919    Lot D6A3020FY    88861799-31    UDI-DI 20884521071060    Lot D6A2861FY",
      "more_code_info": ""
    }
  ]
}