{
  "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": "4452",
      "code_info": "KEB377  KEH280  KGP662  KMJ048  KPP500  LCH042  LHP301  LJE786  LPB869  MAH170  MCH330  MCQ992",
      "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": "PROLENE SUTURE 4-36\"(90CM) 4-0 BLUE, D5988",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ethicon, Inc.",
      "recall_number": "Z-2450-2018",
      "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"
    }
  ]
}