{
  "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": "3024",
      "code_info": "KEH479  KHH259  KLH655  KMH715  LCH548  LHP422  LJJ896  MAR884",
      "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) 3-0 BLUE, D6416",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ethicon, Inc.",
      "recall_number": "Z-2451-2018",
      "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"
    }
  ]
}