{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25470",
      "product_res_number": "Z-0606-03",
      "event_date_initiated": "2002-12-16",
      "event_date_posted": "2003-03-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-10-31",
      "res_event_number": "25255",
      "product_code": "LID",
      "k_numbers": [
        "K910853"
      ],
      "product_description": "External Drainage Sets labeled NMT NeuroSciences Implants or Integra NeuroSciences Implants, S.A.",
      "code_info": "The External Drainage Sets lot numbers:  60300370, 60306608, 60306609, 60321387, 60300373, and 60376191.  These lots of EDS may be included in the following set configurations:  Catalog #:  910-109 Lot#:  0118080; 0118369; 0118572; 0118981; 0119845; 0117525.  Catalog#  910-110A Lot #:  60300370; 60300373; 60306608; 60300370-1; 60321387; 60306608-1; 60306609; 60321387-1; 60306609-1; 60321387-2; 60376191; 60321387-3.  Catalog# 910-112A Lot #:  0117569; 0117609; 0117834; 0117478; 0117833; 0117957; 0118062; 0118175; 0118420; 0118421; 0118573; 0118693.  Catalog #910-118A Lot#:  0117570; 0117479; 0118023; 0118489; 0119150; 0119505.  Catalog #910-120A Lot #:  0117536; 0117371; 0117453; 0117537; 0117902; 0117948; 0118047; 0118161; 0118422; 0118543; 0118616; 0118744; 0118808; 0118912; 0118955; 0119020; 0119081; 0119348; 0119500; 0119582.  Catalog #910-123A Lot #:  0117805; 0118576; 0118845; 0118957.",
      "firm_fei_number": "1121308",
      "recalling_firm": "Integra LifeSciences Corp",
      "address_1": "105 Morgan Lane",
      "city": "Plainsboro",
      "state": "NJ",
      "postal_code": "08536",
      "additional_info_contact": "Donna Wallace, RAC\n609-936-2397",
      "reason_for_recall": "The check valve in the patient line may stick in the closed position.",
      "root_cause_description": "Other",
      "action": "Integra notified their customers via recall letter and reply form on 12/16/2002 via FedEx.",
      "product_quantity": "8952",
      "distribution_pattern": "The affected products have been distributed to hospitals, distributors, and Integra Sales Representatives.  There are 202 direct hospital customers, 5 foreign distributors, and 1 wholesaler.  Government distribution include the National Institute of Health in Bethesda, MD and 9 Veterans Administration Hospitals.  International distributions to the following countries:  United Arab Emirates, Argentina, Australia, Austria, Belgium, Brazil, Canada, Switzerland, Germany, Spain,  France, Gabron, United Kingdom, Greece, Hong Kong, Ireland, Italy, Malaysia, Netherlands, Poland, Saudi Arabia, Sweden, Turkey, South Africa, and Mexico.",
      "openfda": {}
    }
  ]
}