{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Somerville",
      "address_1": "Us Highway 22 West",
      "reason_for_recall": "The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare  professional handling the subject product or a patient infection due to a breach of sterility within the packaging if  it goes unnoticed by the healthcare professional.",
      "address_2": "",
      "product_quantity": "516",
      "code_info": "KDQ147  KEJ159  KGH788",
      "center_classification_date": "20180717",
      "distribution_pattern": "Accounts in AZ, CA, CO, FL, GA, IL, IN, KS, MA, MN, MO, NC, NE, NJ, NY, OH, OR, SC, SD, TN, TX, VA, WA, WI, WV.",
      "state": "NJ",
      "product_description": "PRONOVA SUTURE BLUE 122CM M1.5, D10189",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ethicon, Inc.",
      "recall_number": "Z-2466-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80306",
      "termination_date": "20200608",
      "more_code_info": "",
      "recall_initiation_date": "20180507",
      "postal_code": "08876",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}