{
  "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": "2026-09-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "event_date_initiated": "2002-11-13",
      "event_date_created": "2002-12-02",
      "city": "Lakewood",
      "address_1": "10810 West Collins Ave.",
      "reason_for_recall": "Gambro's ClinicalKit 15G safety Kits contain the Nipro Safetouch Safety Fistula Needles currently being recalled by Nipro for leakage problems",
      "openfda": {},
      "recalling_firm": "Gambro Renal Products",
      "product_res_number": "Z-0307-03",
      "code_info": "Gambro ClinicalKit Safety Kit 15G.  Catalog No. 0141080405C. Lots 05H154001, 04H154007, 04H154010, 04H154011..",
      "product_quantity": "2,160 kits",
      "recall_status": "Completed",
      "res_event_number": "25023",
      "action": "All consignees were notified by telephone and fax on 11/13/2002.",
      "distribution_pattern": "Domestic distribution to CO, IL, MO and VA.  No military, government or foreign consignees.",
      "product_description": "Gambro ClinicalKit Safety Kit 15G, Catalog Number 0141080405C. Packaged 30 kits per case. Each kit contains 2 Nipro Safetouch Safety Needles.",
      "postal_code": "80215"
    }
  ]
}